8-134269012-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134269012
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134269012
    reference: chr 8
allele count: 2
allele frequency: 1.69940860580518e-5
allele num: 117688
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.537+8G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.255+8G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.537+8G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.327+8G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.294+8G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-14713G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.537+8G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*143+8G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.339+8G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-10106G>A
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1996
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33401
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1787
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13527
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6271
  bin: 9.75e1
  variant carriers: 2
hgvs: c.537+8G>A
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

http://identifiers.org/exac.variant/8-134269013-A-AC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134269013
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134269014
    reference: chr 8
allele count: 1
allele frequency: 8.491415179253775e-6
allele num: 117766
alternate allele: AC
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.294+6dupG
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.537+6dupG
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-10108dupG
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.537+6dupG
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.327+6dupG
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.339+6dupG
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.255+6dupG
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-14715dupG
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*143+6dupG
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.537+6dupG
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33407
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13600
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1745
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2382
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2173
  bin: 2.25e1
  variant carriers: 0
hgvs: c.537+6dupG
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

http://identifiers.org/exac.variant/8-134269014-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134269014
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134269014
    reference: chr 8
allele count: 1
allele frequency: 8.483635067953916e-6
allele num: 117874
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.537+6G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.537+6G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.327+6G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-10108G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-14715G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.255+6G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.537+6G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.294+6G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*143+6G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.339+6G>T
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33502
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13631
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 482
  bin: 3.75e1
  variant carriers: 0
hgvs: c.537+6G>T
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

8-134269028-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134269028
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134269028
    reference: chr 8
allele count: 1
allele frequency: 8.414391976035812e-6
allele num: 118844
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-14729G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.319G>A
  hgvsp: ENSP00000347028.5:p.Ala107Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: incomplete_terminal_codon_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.580G>A
  hgvsp: ENST00000520230.1:c.580G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.529G>A
  hgvsp: ENSP00000429380.1:p.Ala177Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.529G>A
  hgvsp: ENSP00000404854.2:p.Ala177Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.529G>A
  hgvsp: ENSP00000319977.7:p.Ala177Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.331G>A
  hgvsp: ENSP00000427894.1:p.Ala111Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.286G>A
  hgvsp: ENSP00000437443.1:p.Ala96Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-10122G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.247G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*135G>A
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2531
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33637
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14526
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala177Thr
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-134269029-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134269029
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134269029
    reference: chr 8
allele count: 5
allele frequency: 4.201468833504193e-5
allele num: 119006
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*134C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-14730C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.528C>T
  hgvsp: ENST00000323851.7:c.528C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.246C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.330C>T
  hgvsp: ENST00000522476.1:c.330C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.528C>T
  hgvsp: ENST00000414097.2:c.528C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.318C>T
  hgvsp: ENST00000354944.5:c.318C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.579C>T
  hgvsp: ENST00000520230.1:c.579C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.285C>T
  hgvsp: ENST00000537882.1:c.285C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.528C>T
  hgvsp: ENST00000522377.1:c.528C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-10123C>T
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14645
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33745
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala176Ala
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

8-134269029-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134269029
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134269029
    reference: chr 8
allele count: 5
allele frequency: 4.201468833504193e-5
allele num: 119006
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.246C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-14730C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.330C>G
  hgvsp: ENST00000522476.1:c.330C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.528C>G
  hgvsp: ENST00000414097.2:c.528C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.528C>G
  hgvsp: ENST00000522377.1:c.528C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.579C>G
  hgvsp: ENST00000520230.1:c.579C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.318C>G
  hgvsp: ENST00000354944.5:c.318C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.528C>G
  hgvsp: ENST00000323851.7:c.528C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*134C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.285C>G
  hgvsp: ENST00000537882.1:c.285C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-10123C>G
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14645
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33745
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2509
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala176Ala
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

8-134269044-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134269044
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134269044
    reference: chr 8
allele count: 1
allele frequency: 8.357011532675915e-6
allele num: 119660
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*119C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.564C>T
  hgvsp: ENST00000520230.1:c.564C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.270C>T
  hgvsp: ENST00000537882.1:c.270C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.513C>T
  hgvsp: ENST00000522377.1:c.513C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.315C>T
  hgvsp: ENST00000522476.1:c.315C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.231C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.513C>T
  hgvsp: ENST00000323851.7:c.513C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.513C>T
  hgvsp: ENST00000414097.2:c.513C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-14745C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.303C>T
  hgvsp: ENST00000354944.5:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-10138C>T
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34017
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15285
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly171Gly
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP

8-134269044-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134269044
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134269044
    reference: chr 8
allele count: 1
allele frequency: 8.357011532675915e-6
allele num: 119660
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.513C>A
  hgvsp: ENST00000522377.1:c.513C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*119C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.513C>A
  hgvsp: ENST00000323851.7:c.513C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.513C>A
  hgvsp: ENST00000414097.2:c.513C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-14745C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.270C>A
  hgvsp: ENST00000537882.1:c.270C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.303C>A
  hgvsp: ENST00000354944.5:c.303C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.564C>A
  hgvsp: ENST00000520230.1:c.564C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.315C>A
  hgvsp: ENST00000522476.1:c.315C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-10138C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.231C>A
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34017
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15285
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly171Gly
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: QD

8-134269050-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134269050
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134269050
    reference: chr 8
allele count: 441
allele frequency: 3.681995792004809e-3
allele num: 119772
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.297G>A
  hgvsp: ENST00000354944.5:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.507G>A
  hgvsp: ENST00000522377.1:c.507G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.225G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.507G>A
  hgvsp: ENST00000414097.2:c.507G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*113G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-10144G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.558G>A
  hgvsp: ENST00000520230.1:c.558G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.309G>A
  hgvsp: ENST00000522476.1:c.309G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-14751G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.507G>A
  hgvsp: ENST00000323851.7:c.507G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.264G>A
  hgvsp: ENST00000537882.1:c.264G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33776
  bin: 2.25e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 1.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 9.75e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 5.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 5.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 7.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 6.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2622
  bin: 3.25e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 3.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 6.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 8.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 4.75e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 15406
  bin: 2.75e1
  variant carriers: 50
genotype quality: GenotypeQuality
hgvs: p.Ala169Ala
num of homozygotes: 2
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: African
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP

8-134269062-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134269062
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134269062
    reference: chr 8
allele count: 1
allele frequency: 8.359107247345984e-6
allele num: 119630
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.297G>A
  hgvsp: ENST00000522476.1:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.546G>A
  hgvsp: ENST00000520230.1:c.546G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*101G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.495G>A
  hgvsp: ENST00000323851.7:c.495G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.297G>A
  hgvsp: ENST00000518480.1:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.252G>A
  hgvsp: ENST00000537882.1:c.252G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.495G>A
  hgvsp: ENST00000522377.1:c.495G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.571G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.285G>A
  hgvsp: ENST00000354944.5:c.285G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-14763G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.213G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.495G>A
  hgvsp: ENST00000519228.1:c.495G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-10156G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.495G>A
  hgvsp: ENST00000414097.2:c.495G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33305
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15789
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val165Val
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

8-134269064-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134269064
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134269064
    reference: chr 8
allele count: 1
allele frequency: 8.366660531115611e-6
allele num: 119522
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.493G>A
  hgvsp: ENSP00000404854.2:p.Val165Met
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.295G>A
  hgvsp: ENSP00000427894.1:p.Val99Met
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.493G>A
  hgvsp: ENSP00000429994.1:p.Val165Met
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.544G>A
  hgvsp: ENSP00000428345.1:p.Val182Met
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.569G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.295G>A
  hgvsp: ENSP00000428802.1:p.Val99Met
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.493G>A
  hgvsp: ENSP00000429380.1:p.Val165Met
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.250G>A
  hgvsp: ENSP00000437443.1:p.Val84Met
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-14765G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.283G>A
  hgvsp: ENSP00000347028.5:p.Val95Met
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*99G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-10158G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.493G>A
  hgvsp: ENSP00000319977.7:p.Val165Met
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.211G>A
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2621
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15813
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33106
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val165Met
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

8-134269065-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134269065
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134269065
    reference: chr 8
allele count: 2
allele frequency: 1.673976363453748e-5
allele num: 119476
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.492C>T
  hgvsp: ENST00000522377.1:c.492C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.543C>T
  hgvsp: ENST00000520230.1:c.543C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.282C>T
  hgvsp: ENST00000354944.5:c.282C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.294C>T
  hgvsp: ENST00000518480.1:c.294C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.294C>T
  hgvsp: ENST00000522476.1:c.294C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.249C>T
  hgvsp: ENST00000537882.1:c.249C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.492C>T
  hgvsp: ENST00000323851.7:c.492C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.568C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.492C>T
  hgvsp: ENST00000519228.1:c.492C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*98C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-10159C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-14766C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.492C>T
  hgvsp: ENST00000414097.2:c.492C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.210C>T
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33059
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2587
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn164Asn
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

8-134269069-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134269069
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134269069
    reference: chr 8
allele count: 1
allele frequency: 8.378296859814337e-6
allele num: 119356
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.290T>C
  hgvsp: ENSP00000427894.1:p.Ile97Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.488T>C
  hgvsp: ENSP00000429994.1:p.Ile163Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.488T>C
  hgvsp: ENSP00000429380.1:p.Ile163Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.488T>C
  hgvsp: ENSP00000319977.7:p.Ile163Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.488T>C
  hgvsp: ENSP00000404854.2:p.Ile163Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-10163T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.290T>C
  hgvsp: ENSP00000428802.1:p.Ile97Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-14770T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*94T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.206T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.245T>C
  hgvsp: ENSP00000437443.1:p.Ile82Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.539T>C
  hgvsp: ENSP00000428345.1:p.Ile180Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.278T>C
  hgvsp: ENSP00000347028.5:p.Ile93Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.564T>C
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2571
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15771
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32826
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile163Thr
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum

8-134269073-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134269073
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134269073
    reference: chr 8
allele count: 1
allele frequency: 8.392641332080031e-6
allele num: 119152
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.484C>G
  hgvsp: ENSP00000404854.2:p.Leu162Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.286C>G
  hgvsp: ENSP00000428802.1:p.Leu96Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.484C>G
  hgvsp: ENSP00000429994.1:p.Leu162Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.484C>G
  hgvsp: ENSP00000429380.1:p.Leu162Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.274C>G
  hgvsp: ENSP00000347028.5:p.Leu92Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.560C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*90C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.241C>G
  hgvsp: ENSP00000437443.1:p.Leu81Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.535C>G
  hgvsp: ENSP00000428345.1:p.Leu179Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.286C>G
  hgvsp: ENSP00000427894.1:p.Leu96Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-10167C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-14774C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.202C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.484C>G
  hgvsp: ENSP00000319977.7:p.Leu162Val
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32630
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu162Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

8-134269074-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134269074
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134269074
    reference: chr 8
allele count: 1
allele frequency: 8.397151686148059e-6
allele num: 119088
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.240C>A
  hgvsp: ENST00000537882.1:c.240C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.559C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.201C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.285C>A
  hgvsp: ENST00000522476.1:c.285C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*89C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.273C>A
  hgvsp: ENST00000354944.5:c.273C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.285C>A
  hgvsp: ENST00000518480.1:c.285C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.483C>A
  hgvsp: ENST00000519228.1:c.483C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.534C>A
  hgvsp: ENST00000520230.1:c.534C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.483C>A
  hgvsp: ENST00000522377.1:c.483C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.483C>A
  hgvsp: ENST00000414097.2:c.483C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-10168C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-14775C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.483C>A
  hgvsp: ENST00000323851.7:c.483C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32609
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val161Val
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum

8-134269080-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134269080
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134269080
    reference: chr 8
allele count: 3
allele frequency: 2.526315789473684e-5
allele num: 118750
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.195C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*83C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.477C>T
  hgvsp: ENST00000519228.1:c.477C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.477C>T
  hgvsp: ENST00000414097.2:c.477C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.279C>T
  hgvsp: ENST00000522476.1:c.279C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.477C>T
  hgvsp: ENST00000522377.1:c.477C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.477C>T
  hgvsp: ENST00000323851.7:c.477C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.234C>T
  hgvsp: ENST00000537882.1:c.234C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.279C>T
  hgvsp: ENST00000518480.1:c.279C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.267C>T
  hgvsp: ENST00000354944.5:c.267C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-10174C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-14781C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.528C>T
  hgvsp: ENST00000520230.1:c.528C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.553C>T
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15466
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly159Gly
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum

8-134269081-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134269081
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134269081
    reference: chr 8
allele count: 1
allele frequency: 8.426871608184177e-6
allele num: 118668
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.278G>A
  hgvsp: ENSP00000427894.1:p.Gly93Asp
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.527G>A
  hgvsp: ENSP00000428345.1:p.Gly176Asp
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.476G>A
  hgvsp: ENSP00000429994.1:p.Gly159Asp
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.476G>A
  hgvsp: ENSP00000404854.2:p.Gly159Asp
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-10175G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.552G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.233G>A
  hgvsp: ENSP00000437443.1:p.Gly78Asp
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.476G>A
  hgvsp: ENSP00000319977.7:p.Gly159Asp
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-14782G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.476G>A
  hgvsp: ENSP00000429380.1:p.Gly159Asp
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.194G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.278G>A
  hgvsp: ENSP00000428802.1:p.Gly93Asp
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.266G>A
  hgvsp: ENSP00000347028.5:p.Gly89Asp
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*82G>A
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15459
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32128
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gly159Asp
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP

8-134269088-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134269088
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134269088
    reference: chr 8
allele count: 1
allele frequency: 8.477162524159914e-6
allele num: 117964
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.469G>A
  hgvsp: ENSP00000404854.2:p.Val157Met
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.271G>A
  hgvsp: ENSP00000427894.1:p.Val91Met
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.520G>A
  hgvsp: ENSP00000428345.1:p.Val174Met
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-10182G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.469G>A
  hgvsp: ENSP00000429380.1:p.Val157Met
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.469G>A
  hgvsp: ENSP00000319977.7:p.Val157Met
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.469G>A
  hgvsp: ENSP00000429272.1:p.Val157Met
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.469G>A
  hgvsp: ENSP00000428384.1:p.Val157Met
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.469G>A
  hgvsp: ENSP00000429994.1:p.Val157Met
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-14789G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*75G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.187G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.271G>A
  hgvsp: ENSP00000428802.1:p.Val91Met
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.545G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.226G>A
  hgvsp: ENSP00000437443.1:p.Val76Met
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.259G>A
  hgvsp: ENSP00000347028.5:p.Val87Met
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31073
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2476
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val157Met
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

8-134269101-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134269101
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134269101
    reference: chr 8
allele count: 1
allele frequency: 8.647227698799765e-6
allele num: 115644
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.213C>G
  hgvsp: ENSP00000437443.1:p.Asn71Lys
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.258C>G
  hgvsp: ENSP00000428802.1:p.Asn86Lys
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.507C>G
  hgvsp: ENSP00000428345.1:p.Asn169Lys
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.456C>G
  hgvsp: ENSP00000404854.2:p.Asn152Lys
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.456C>G
  hgvsp: ENSP00000428384.1:p.Asn152Lys
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.456C>G
  hgvsp: ENSP00000429272.1:p.Asn152Lys
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.456C>G
  hgvsp: ENSP00000429380.1:p.Asn152Lys
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-14802C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.246C>G
  hgvsp: ENSP00000347028.5:p.Asn82Lys
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.258C>G
  hgvsp: ENSP00000427894.1:p.Asn86Lys
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.456C>G
  hgvsp: ENSP00000319977.7:p.Asn152Lys
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.456C>G
  hgvsp: ENSP00000429994.1:p.Asn152Lys
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.532C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-10195C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.174C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*62C>G
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27741
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4894
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn152Lys
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: African
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: FS

8-134269102-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134269102
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134269102
    reference: chr 8
allele count: 2
allele frequency: 1.73178165696869e-5
allele num: 115488
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.455A>C
  hgvsp: ENSP00000404854.2:p.Asn152Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.531A>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.455A>C
  hgvsp: ENSP00000429380.1:p.Asn152Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.506A>C
  hgvsp: ENSP00000428345.1:p.Asn169Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.173A>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-14803A>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-10196A>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.455A>C
  hgvsp: ENSP00000429272.1:p.Asn152Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.455A>C
  hgvsp: ENSP00000319977.7:p.Asn152Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.257A>C
  hgvsp: ENSP00000427894.1:p.Asn86Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.455A>C
  hgvsp: ENSP00000428384.1:p.Asn152Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.245A>C
  hgvsp: ENSP00000347028.5:p.Asn82Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*61A>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.212A>C
  hgvsp: ENSP00000437443.1:p.Asn71Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.455A>C
  hgvsp: ENSP00000429994.1:p.Asn152Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.257A>C
  hgvsp: ENSP00000428802.1:p.Asn86Thr
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14605
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2887
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn152Thr
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum

8-134269104-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134269104
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134269104
    reference: chr 8
allele count: 3
allele frequency: 2.610875165355427e-5
allele num: 114904
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.243A>G
  hgvsp: ENST00000354944.5:c.243A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.255A>G
  hgvsp: ENST00000518480.1:c.255A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*59A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-10198A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-14805A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.255A>G
  hgvsp: ENST00000522476.1:c.255A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.453A>G
  hgvsp: ENST00000323851.7:c.453A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.529A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.210A>G
  hgvsp: ENST00000537882.1:c.210A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.171A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.453A>G
  hgvsp: ENST00000522377.1:c.453A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.453A>G
  hgvsp: ENST00000519228.1:c.453A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.504A>G
  hgvsp: ENST00000520230.1:c.504A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.453A>G
  hgvsp: ENST00000522890.1:c.453A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.453A>G
  hgvsp: ENST00000519580.1:c.453A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.453A>G
  hgvsp: ENST00000414097.2:c.453A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.453A>G
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

8-134269107-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134269107
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134269107
    reference: chr 8
allele count: 1
allele frequency: 8.747681864305959e-6
allele num: 114316
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.451-1G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*57-1G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.527-1G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.208-1G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.253-1G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.451-1G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.241-1G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-14808G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.451-1G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.451-1G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.169-1G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.253-1G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.502-1G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.451-1G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.451-1G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-10201G>C
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3428
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.451-1G>C
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum

8-134269109-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134269109
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134269109
    reference: chr 8
allele count: 1
allele frequency: 8.800957544180806e-6
allele num: 113624
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.451-3C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.241-3C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.253-3C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-10203C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.451-3C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.451-3C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.502-3C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.451-3C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.451-3C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.527-3C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.169-3C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*57-3C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.253-3C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-14810C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.451-3C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.208-3C>T
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13711
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7615
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.451-3C>T
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD

8-134269110-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134269110
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134269110
    reference: chr 8
allele count: 1
allele frequency: 8.847521809141259e-6
allele num: 113026
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.527-4G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.451-4G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.253-4G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.502-4G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.451-4G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*57-4G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-14811G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.451-4G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-10204G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.451-4G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.451-4G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.253-4G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.169-4G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.451-4G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.208-4G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.241-4G>A
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8733
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.451-4G>A
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

8-134269113-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134269113
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134269113
    reference: chr 8
allele count: 1
allele frequency: 8.859907148173087e-6
allele num: 112868
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.451-7A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.527-7A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.253-7A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.253-7A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.241-7A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-14814A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.502-7A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.451-7A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.208-7A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.169-7A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-10207A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*57-7A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.451-7A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.451-7A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.451-7A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.451-7A>G
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2184
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23133
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.451-7A>G
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

8-134269134-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134269134
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134269134
    reference: chr 8
allele count: 1
allele frequency: 9.363120540813842e-6
allele num: 106802
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.169-28C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.208-28C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.451-28C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.527-28C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.451-28C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.253-28C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.451-28C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*57-28C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-10228C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.451-28C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.502-28C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.451-28C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.253-28C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.451-28C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-14835C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.241-28C>A
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21468
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9302
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7860
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: DP

8-134269138-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134269138
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134269137
    reference: chr 8
allele count: 2
allele frequency: 1.902225603956629e-5
allele num: 105140
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-14840delG
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.451-33delG
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.208-33delG
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.253-33delG
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.502-33delG
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.451-33delG
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.451-33delG
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.169-33delG
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.451-33delG
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.241-33delG
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.527-33delG
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.451-33delG
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*57-33delG
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-10233delG
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.253-33delG
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.451-33delG
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6958
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5367
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10254
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7011
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: TC
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: DP

8-134269157-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134269157
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134269157
    reference: chr 8
allele count: 1
allele frequency: 1.050530517911545e-5
allele num: 95190
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.253-51A>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.253-51A>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.451-51A>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.451-51A>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.241-51A>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.451-51A>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-14858A>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.451-51A>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-10251A>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.451-51A>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*57-51A>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.451-51A>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.169-51A>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.527-51A>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.502-51A>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.208-51A>T
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10912
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19930
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

8-134270565-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134270565
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134270565
    reference: chr 8
allele count: 1
allele frequency: 1.672968180145214e-5
allele num: 59774
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.207+44T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.450+44T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.168+44T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*56+44T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.450+44T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-16266T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-11659T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.450+44T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.526+846T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.240+44T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.501+44T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.252+44T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.252+44T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.450+44T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.450+44T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.450+44T>C
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24400
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6111
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

8-134270580-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134270580
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134270580
    reference: chr 8
allele count: 11
allele frequency: 1.770481248994045e-4
allele num: 62130
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.450+29G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.207+29G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.450+29G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.501+29G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-16281G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.450+29G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.450+29G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.526+831G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.252+29G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.450+29G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.252+29G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.168+29G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*56+29G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.240+29G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-11674G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.450+29G>A
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25981
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

8-134270581-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134270581
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134270581
    reference: chr 8
allele count: 1
allele frequency: 1.583130164962163e-5
allele num: 63166
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*56+28C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.207+28C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.450+28C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-16282C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.450+28C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.450+28C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.450+28C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.450+28C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.252+28C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.168+28C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-11675C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.526+830C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.240+28C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.450+28C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.252+28C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.501+28C>T
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11540
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8872
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25899
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2768
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

8-134270586-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134270586
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134270586
    reference: chr 8
allele count: 2
allele frequency: 3.047108294228777e-5
allele num: 65636
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.240+23A>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.168+23A>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.450+23A>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*56+23A>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-16287A>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.207+23A>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.252+23A>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.450+23A>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.252+23A>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.450+23A>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.501+23A>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.526+825A>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.450+23A>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-11680A>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.450+23A>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.450+23A>C
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25588
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

8-134270597-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134270597
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134270597
    reference: chr 8
allele count: 1
allele frequency: 1.342966882436679e-5
allele num: 74462
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.450+12G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.450+12G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.450+12G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-16298G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.526+814G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.501+12G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.168+12G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.450+12G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.252+12G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*56+12G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.207+12G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.450+12G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-11691G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.450+12G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.240+12G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.252+12G>C
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18717
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6565
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/8-134270611-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134270611
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134270611
    reference: chr 8
allele count: 36
allele frequency: 4.261565415029121e-4
allele num: 84476
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.250G>T
  hgvsp: ENSP00000428802.1:p.Ala84Ser
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.448G>T
  hgvsp: ENSP00000404854.2:p.Ala150Ser
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.448G>T
  hgvsp: ENSP00000429380.1:p.Ala150Ser
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.166G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-11705G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.250G>T
  hgvsp: ENSP00000427894.1:p.Ala84Ser
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.448G>T
  hgvsp: ENSP00000428384.1:p.Ala150Ser
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.499G>T
  hgvsp: ENSP00000428345.1:p.Ala167Ser
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.526+800G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*54G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.448G>T
  hgvsp: ENSP00000429272.1:p.Ala150Ser
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.238G>T
  hgvsp: ENSP00000347028.5:p.Ala80Ser
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.448G>T
  hgvsp: ENSP00000429994.1:p.Ala150Ser
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.448G>T
  hgvsp: ENSP00000319977.7:p.Ala150Ser
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-16312G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.205G>T
  hgvsp: ENSP00000437443.1:p.Ala69Ser
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2924
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4495
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala150Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

8-134270616-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134270616
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134270616
    reference: chr 8
allele count: 1
allele frequency: 1.153721906871568e-5
allele num: 86676
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*49G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.161G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-16317G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.245G>A
  hgvsp: ENSP00000427894.1:p.Arg82Gln
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.443G>A
  hgvsp: ENSP00000429380.1:p.Arg148Gln
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.245G>A
  hgvsp: ENSP00000428802.1:p.Arg82Gln
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-11710G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.443G>A
  hgvsp: ENSP00000319977.7:p.Arg148Gln
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.233G>A
  hgvsp: ENSP00000347028.5:p.Arg78Gln
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.494G>A
  hgvsp: ENSP00000428345.1:p.Arg165Gln
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.443G>A
  hgvsp: ENSP00000404854.2:p.Arg148Gln
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.443G>A
  hgvsp: ENSP00000429994.1:p.Arg148Gln
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.526+795G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.200G>A
  hgvsp: ENSP00000437443.1:p.Arg67Gln
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.443G>A
  hgvsp: ENSP00000428384.1:p.Arg148Gln
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.443G>A
  hgvsp: ENSP00000429272.1:p.Arg148Gln
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4165
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3112
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg148Gln
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: C
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

8-134270626-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134270626
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134270626
    reference: chr 8
allele count: 1
allele frequency: 1.110790216159776e-5
allele num: 90026
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.433A>G
  hgvsp: ENSP00000429994.1:p.Ile145Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-11720A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.235A>G
  hgvsp: ENSP00000428802.1:p.Ile79Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*39A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.433A>G
  hgvsp: ENSP00000428384.1:p.Ile145Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.223A>G
  hgvsp: ENSP00000347028.5:p.Ile75Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.484A>G
  hgvsp: ENSP00000428345.1:p.Ile162Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429840
  ensembl transcript: ENST00000520943
  gene symbol: NDRG1
  hgvsc: ENST00000520943.1:c.466A>G
  hgvsp: ENSP00000429840.1:p.Ile156Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.526+785A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.151A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.190A>G
  hgvsp: ENSP00000437443.1:p.Ile64Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.235A>G
  hgvsp: ENSP00000427894.1:p.Ile79Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.433A>G
  hgvsp: ENSP00000429380.1:p.Ile145Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.433A>G
  hgvsp: ENSP00000404854.2:p.Ile145Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.433A>G
  hgvsp: ENSP00000429272.1:p.Ile145Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-16327A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.433A>G
  hgvsp: ENSP00000319977.7:p.Ile145Val
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26786
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile145Val
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

8-134270627-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134270627
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134270627
    reference: chr 8
allele count: 1
allele frequency: 1.108696616257927e-5
allele num: 90196
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.432C>T
  hgvsp: ENST00000522377.1:c.432C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.432C>T
  hgvsp: ENST00000522890.1:c.432C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.432C>T
  hgvsp: ENST00000414097.2:c.432C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.432C>T
  hgvsp: ENST00000519580.1:c.432C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.234C>T
  hgvsp: ENST00000522476.1:c.234C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*38C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-16328C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.234C>T
  hgvsp: ENST00000518480.1:c.234C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.483C>T
  hgvsp: ENST00000520230.1:c.483C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.526+784C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.222C>T
  hgvsp: ENST00000354944.5:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.432C>T
  hgvsp: ENST00000323851.7:c.432C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.432C>T
  hgvsp: ENST00000519228.1:c.432C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.150C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429840
  ensembl transcript: ENST00000520943
  gene symbol: NDRG1
  hgvsc: ENST00000520943.1:c.465C>T
  hgvsp: ENST00000520943.1:c.465C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-11721C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.189C>T
  hgvsp: ENST00000537882.1:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr144Tyr
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

8-134270628-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134270628
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134270628
    reference: chr 8
allele count: 2
allele frequency: 2.210091276769731e-5
allele num: 90494
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-11722A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.431A>G
  hgvsp: ENSP00000429994.1:p.Tyr144Cys
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.431A>G
  hgvsp: ENSP00000319977.7:p.Tyr144Cys
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.431A>G
  hgvsp: ENSP00000429272.1:p.Tyr144Cys
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.431A>G
  hgvsp: ENSP00000429380.1:p.Tyr144Cys
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.149A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.431A>G
  hgvsp: ENSP00000428384.1:p.Tyr144Cys
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-16329A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.233A>G
  hgvsp: ENSP00000428802.1:p.Tyr78Cys
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.233A>G
  hgvsp: ENSP00000427894.1:p.Tyr78Cys
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*37A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.431A>G
  hgvsp: ENSP00000404854.2:p.Tyr144Cys
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429840
  ensembl transcript: ENST00000520943
  gene symbol: NDRG1
  hgvsc: ENST00000520943.1:c.464A>G
  hgvsp: ENSP00000429840.1:p.Tyr155Cys
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.221A>G
  hgvsp: ENSP00000347028.5:p.Tyr74Cys
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.482A>G
  hgvsp: ENSP00000428345.1:p.Tyr161Cys
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.188A>G
  hgvsp: ENSP00000437443.1:p.Tyr63Cys
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.526+783A>G
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr144Cys
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

8-134270632-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134270632
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134270632
    reference: chr 8
allele count: 1
allele frequency: 1.099311830793923e-5
allele num: 90966
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.229G>A
  hgvsp: ENSP00000428802.1:p.Ala77Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429840
  ensembl transcript: ENST00000520943
  gene symbol: NDRG1
  hgvsc: ENST00000520943.1:c.460G>A
  hgvsp: ENSP00000429840.1:p.Ala154Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.427G>A
  hgvsp: ENSP00000404854.2:p.Ala143Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-16333G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.145G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*33G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.478G>A
  hgvsp: ENSP00000428345.1:p.Ala160Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.526+779G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-11726G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.427G>A
  hgvsp: ENSP00000319977.7:p.Ala143Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.229G>A
  hgvsp: ENSP00000427894.1:p.Ala77Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.427G>A
  hgvsp: ENSP00000429272.1:p.Ala143Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.427G>A
  hgvsp: ENSP00000429380.1:p.Ala143Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.427G>A
  hgvsp: ENSP00000428384.1:p.Ala143Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.427G>A
  hgvsp: ENSP00000429994.1:p.Ala143Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.217G>A
  hgvsp: ENSP00000347028.5:p.Ala73Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.184G>A
  hgvsp: ENSP00000437443.1:p.Ala62Thr
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14702
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4249
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala143Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

8-134270633-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134270633
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134270633
    reference: chr 8
allele count: 1
allele frequency: 1.100158422812885e-5
allele num: 90896
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.216C>T
  hgvsp: ENST00000354944.5:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.228C>T
  hgvsp: ENST00000522476.1:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.228C>T
  hgvsp: ENST00000518480.1:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.426C>T
  hgvsp: ENST00000522377.1:c.426C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-11727C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*32C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.426C>T
  hgvsp: ENST00000519580.1:c.426C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.144C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429840
  ensembl transcript: ENST00000520943
  gene symbol: NDRG1
  hgvsc: ENST00000520943.1:c.459C>T
  hgvsp: ENST00000520943.1:c.459C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.426C>T
  hgvsp: ENST00000522890.1:c.426C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.426C>T
  hgvsp: ENST00000414097.2:c.426C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.477C>T
  hgvsp: ENST00000520230.1:c.477C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.183C>T
  hgvsp: ENST00000537882.1:c.183C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.426C>T
  hgvsp: ENST00000323851.7:c.426C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-16334C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.526+778C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.426C>T
  hgvsp: ENST00000519228.1:c.426C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26597
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4407
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.216C>T
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

8-134270638-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134270638
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134270638
    reference: chr 8
allele count: 7
allele frequency: 7.672241829062452e-5
allele num: 91238
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429840
  ensembl transcript: ENST00000520943
  gene symbol: NDRG1
  hgvsc: ENST00000520943.1:c.454G>A
  hgvsp: ENSP00000429840.1:p.Ala152Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-16339G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.223G>A
  hgvsp: ENSP00000428802.1:p.Ala75Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.421G>A
  hgvsp: ENSP00000404854.2:p.Ala141Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-11732G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.421G>A
  hgvsp: ENSP00000428384.1:p.Ala141Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.526+773G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.223G>A
  hgvsp: ENSP00000427894.1:p.Ala75Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.421G>A
  hgvsp: ENSP00000319977.7:p.Ala141Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.178G>A
  hgvsp: ENSP00000437443.1:p.Ala60Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.421G>A
  hgvsp: ENSP00000429272.1:p.Ala141Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.421G>A
  hgvsp: ENSP00000429994.1:p.Ala141Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.215-4G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.472G>A
  hgvsp: ENSP00000428345.1:p.Ala158Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.421G>A
  hgvsp: ENSP00000429380.1:p.Ala141Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*27G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.139G>A
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4246
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala141Thr
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: C
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

8-134270642-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134270642
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134270642
    reference: chr 8
allele count: 1
allele frequency: 1.098225267966965e-5
allele num: 91056
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.417A>G
  hgvsp: ENST00000519580.1:c.417A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.417A>G
  hgvsp: ENST00000323851.7:c.417A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*23A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.135A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.215-8A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.417A>G
  hgvsp: ENST00000522890.1:c.417A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.417A>G
  hgvsp: ENST00000519228.1:c.417A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.526+769A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-11736A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.417A>G
  hgvsp: ENST00000522377.1:c.417A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.174A>G
  hgvsp: ENST00000537882.1:c.174A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.417A>G
  hgvsp: ENST00000414097.2:c.417A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.219A>G
  hgvsp: ENST00000522476.1:c.219A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-16343A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.219A>G
  hgvsp: ENST00000518480.1:c.219A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429840
  ensembl transcript: ENST00000520943
  gene symbol: NDRG1
  hgvsc: ENST00000520943.1:c.450A>G
  hgvsp: ENST00000520943.1:c.450A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.468A>G
  hgvsp: ENST00000520230.1:c.468A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25491
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4364
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.215-8A>G
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-134270645-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134270645
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134270645
    reference: chr 8
allele count: 1
allele frequency: 1.104777055990101e-5
allele num: 90516
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.526+766A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.216A>G
  hgvsp: ENST00000522476.1:c.216A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.414A>G
  hgvsp: ENST00000323851.7:c.414A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429840
  ensembl transcript: ENST00000520943
  gene symbol: NDRG1
  hgvsc: ENST00000520943.1:c.447A>G
  hgvsp: ENST00000520943.1:c.447A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-11739A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.216A>G
  hgvsp: ENST00000518480.1:c.216A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.465A>G
  hgvsp: ENST00000520230.1:c.465A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.414A>G
  hgvsp: ENST00000519580.1:c.414A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.414A>G
  hgvsp: ENST00000522890.1:c.414A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.171A>G
  hgvsp: ENST00000537882.1:c.171A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.215-11A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*20A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.414A>G
  hgvsp: ENST00000414097.2:c.414A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.414A>G
  hgvsp: ENST00000519228.1:c.414A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.132A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.414A>G
  hgvsp: ENST00000522377.1:c.414A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-16346A>G
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6074
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4426
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gly138Gly
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ

8-134270650-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134270650
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134270650
    reference: chr 8
allele count: 8
allele frequency: 9.044453488897933e-5
allele num: 88452
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*15A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.409A>G
  hgvsp: ENSP00000319977.7:p.Met137Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.215-16A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.409A>G
  hgvsp: ENSP00000429380.1:p.Met137Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.211A>G
  hgvsp: ENSP00000428802.1:p.Met71Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.526+761A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-16351A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.409A>G
  hgvsp: ENSP00000428384.1:p.Met137Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-11744A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.166A>G
  hgvsp: ENSP00000437443.1:p.Met56Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.409A>G
  hgvsp: ENSP00000429272.1:p.Met137Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.409A>G
  hgvsp: ENSP00000404854.2:p.Met137Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.211A>G
  hgvsp: ENSP00000427894.1:p.Met71Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.460A>G
  hgvsp: ENSP00000428345.1:p.Met154Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.409A>G
  hgvsp: ENSP00000429994.1:p.Met137Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.127A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429840
  ensembl transcript: ENST00000520943
  gene symbol: NDRG1
  hgvsc: ENST00000520943.1:c.442A>G
  hgvsp: ENSP00000429840.1:p.Met148Val
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21248
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met137Val
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: South Asian
reference allele: T
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

8-134270656-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134270656
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134270656
    reference: chr 8
allele count: 28
allele frequency: 3.21853878339234e-4
allele num: 86996
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.205A>G
  hgvsp: ENSP00000428802.1:p.Ile69Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.160A>G
  hgvsp: ENSP00000437443.1:p.Ile54Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-11750A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.403A>G
  hgvsp: ENSP00000428384.1:p.Ile135Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*9A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.403A>G
  hgvsp: ENSP00000404854.2:p.Ile135Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.454A>G
  hgvsp: ENSP00000428345.1:p.Ile152Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.403A>G
  hgvsp: ENSP00000319977.7:p.Ile135Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-16357A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.403A>G
  hgvsp: ENSP00000429380.1:p.Ile135Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.205A>G
  hgvsp: ENSP00000427894.1:p.Ile69Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.403A>G
  hgvsp: ENSP00000429272.1:p.Ile135Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.403A>G
  hgvsp: ENSP00000429994.1:p.Ile135Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.526+755A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.215-22A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.121A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429840
  ensembl transcript: ENST00000520943
  gene symbol: NDRG1
  hgvsc: ENST00000520943.1:c.436A>G
  hgvsp: ENSP00000429840.1:p.Ile146Val
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16336
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile135Val
num of homozygotes: 1
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

8-134270659-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134270659
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134270659
    reference: chr 8
allele count: 3
allele frequency: 3.49585158944719e-5
allele num: 85816
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.400A>G
  hgvsp: ENSP00000428384.1:p.Ile134Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.400A>G
  hgvsp: ENSP00000319977.7:p.Ile134Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.400A>G
  hgvsp: ENSP00000429994.1:p.Ile134Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.400A>G
  hgvsp: ENSP00000429380.1:p.Ile134Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.215-25A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.157A>G
  hgvsp: ENSP00000437443.1:p.Ile53Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.202A>G
  hgvsp: ENSP00000427894.1:p.Ile68Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.400A>G
  hgvsp: ENSP00000404854.2:p.Ile134Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.400A>G
  hgvsp: ENSP00000429272.1:p.Ile134Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429840
  ensembl transcript: ENST00000520943
  gene symbol: NDRG1
  hgvsc: ENST00000520943.1:c.433A>G
  hgvsp: ENSP00000429840.1:p.Ile145Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.202A>G
  hgvsp: ENSP00000428802.1:p.Ile68Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.526+752A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-16360A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: incomplete_terminal_codon_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429524
  ensembl transcript: ENST00000521544
  gene symbol: NDRG1
  hgvsc: ENST00000521544.1:c.400A>G
  hgvsp: ENST00000521544.1:c.400A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.*6A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.118A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-11753A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.451A>G
  hgvsp: ENSP00000428345.1:p.Ile151Val
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10815
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ile134Val
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-134270665-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134270665
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134270665
    reference: chr 8
allele count: 1
allele frequency: 1.199127035518143e-5
allele num: 83394
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.196A>C
  hgvsp: ENSP00000427894.1:p.Lys66Gln
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.394A>C
  hgvsp: ENSP00000428384.1:p.Lys132Gln
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-16366A>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.394A>C
  hgvsp: ENSP00000404854.2:p.Lys132Gln
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: stop_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.288A>C
  hgvsp: ENSP00000429172.1:p.Ter96CysextTer15
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.394A>C
  hgvsp: ENSP00000429994.1:p.Lys132Gln
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-11759A>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.215-31A>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.151A>C
  hgvsp: ENSP00000437443.1:p.Lys51Gln
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.445A>C
  hgvsp: ENSP00000428345.1:p.Lys149Gln
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.394A>C
  hgvsp: ENSP00000319977.7:p.Lys132Gln
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.196A>C
  hgvsp: ENSP00000428802.1:p.Lys66Gln
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429524
  ensembl transcript: ENST00000521544
  gene symbol: NDRG1
  hgvsc: ENST00000521544.1:c.394A>C
  hgvsp: ENSP00000429524.1:p.Lys132Gln
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.526+746A>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429840
  ensembl transcript: ENST00000520943
  gene symbol: NDRG1
  hgvsc: ENST00000520943.1:c.427A>C
  hgvsp: ENSP00000429840.1:p.Lys143Gln
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.394A>C
  hgvsp: ENSP00000429380.1:p.Lys132Gln
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.112A>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.394A>C
  hgvsp: ENSP00000429272.1:p.Lys132Gln
  variant of: http://identifiers.org/hgnc/7679
canonical: false
consequence: stop lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ter96CysextTer15
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff

8-134270666-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134270666
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134270666
    reference: chr 8
allele count: 11
allele frequency: 1.326483853073825e-4
allele num: 82926
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.215-32G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429524
  ensembl transcript: ENST00000521544
  gene symbol: NDRG1
  hgvsc: ENST00000521544.1:c.393G>A
  hgvsp: ENST00000521544.1:c.393G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.150G>A
  hgvsp: ENST00000537882.1:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.393G>A
  hgvsp: ENST00000519228.1:c.393G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: stop_retained_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.287G>A
  hgvsp: ENST00000517599.1:c.287G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.111G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-16367G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.195G>A
  hgvsp: ENST00000522476.1:c.195G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.526+745G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429840
  ensembl transcript: ENST00000520943
  gene symbol: NDRG1
  hgvsc: ENST00000520943.1:c.426G>A
  hgvsp: ENST00000520943.1:c.426G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.444G>A
  hgvsp: ENST00000520230.1:c.444G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.393G>A
  hgvsp: ENST00000323851.7:c.393G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.393G>A
  hgvsp: ENST00000522377.1:c.393G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.393G>A
  hgvsp: ENST00000522890.1:c.393G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-11760G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.393G>A
  hgvsp: ENST00000414097.2:c.393G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.393G>A
  hgvsp: ENST00000519580.1:c.393G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.195G>A
  hgvsp: ENST00000518480.1:c.195G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
canonical: false
consequence: stop retained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17714
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ter96Ter
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/8-134270685-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134270685
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134270685
    reference: chr 8
allele count: 1
allele frequency: 1.29769011160135e-5
allele num: 77060
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429840
  ensembl transcript: ENST00000520943
  gene symbol: NDRG1
  hgvsc: ENST00000520943.1:c.423-16G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.215-51G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.390-16G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429524
  ensembl transcript: ENST00000521544
  gene symbol: NDRG1
  hgvsc: ENST00000521544.1:c.390-16G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.284-16G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.390-16G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.147-16G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.526+726G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.108-16G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-16386G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.390-16G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.390-16G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-11779G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.192-16G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.192-16G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.441-16G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.390-16G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.390-16G>T
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2774
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQ

8-134270688-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134270688
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134270688
    reference: chr 8
allele count: 1
allele frequency: 1.310375553633671e-5
allele num: 76314
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.390-19T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429840
  ensembl transcript: ENST00000520943
  gene symbol: NDRG1
  hgvsc: ENST00000520943.1:c.423-19T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.390-19T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.147-19T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.390-19T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.526+723T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-16389T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.441-19T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.390-19T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.284-19T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429524
  ensembl transcript: ENST00000521544
  gene symbol: NDRG1
  hgvsc: ENST00000521544.1:c.390-19T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-11782T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.108-19T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.192-19T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.390-19T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.390-19T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.215-54T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.192-19T>C
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2939
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5346
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: DP

8-134270690-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134270690
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134270690
    reference: chr 8
allele count: 1
allele frequency: 1.327245699723933e-5
allele num: 75344
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.390-21C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.192-21C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.192-21C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429524
  ensembl transcript: ENST00000521544
  gene symbol: NDRG1
  hgvsc: ENST00000521544.1:c.390-21C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.390-21C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-11784C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.390-21C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-16391C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429840
  ensembl transcript: ENST00000520943
  gene symbol: NDRG1
  hgvsc: ENST00000520943.1:c.423-21C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.108-21C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.284-21C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.526+721C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.215-56C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.147-21C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.390-21C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.390-21C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.441-21C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.390-21C>G
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4723
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

8-134270701-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134270701
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134270701
    reference: chr 8
allele count: 1
allele frequency: 1.43000143000143e-5
allele num: 69930
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.390-32T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.147-32T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.390-32T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.284-32T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.192-32T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.390-32T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.108-32T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.215-67T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429840
  ensembl transcript: ENST00000520943
  gene symbol: NDRG1
  hgvsc: ENST00000520943.1:c.423-32T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429524
  ensembl transcript: ENST00000521544
  gene symbol: NDRG1
  hgvsc: ENST00000521544.1:c.390-32T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.390-32T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-11795T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.192-32T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.390-32T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.390-32T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.526+710T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.441-32T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-16402T>C
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5461
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

8-134270701-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134270701
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134270701
    reference: chr 8
allele count: 7
allele frequency: 1.001001001001001e-4
allele num: 69930
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.526+710T>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-16402T>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.390-32T>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.284-32T>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.441-32T>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429840
  ensembl transcript: ENST00000520943
  gene symbol: NDRG1
  hgvsc: ENST00000520943.1:c.423-32T>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.192-32T>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.390-32T>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.192-32T>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.108-32T>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429524
  ensembl transcript: ENST00000521544
  gene symbol: NDRG1
  hgvsc: ENST00000521544.1:c.390-32T>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.147-32T>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.390-32T>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.390-32T>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.390-32T>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.390-32T>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.215-67T>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-11795T>A
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19815
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3745
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum

8-134270703-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134270703
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134270703
    reference: chr 8
allele count: 860
allele frequency: 1.261848167385627e-2
allele num: 68154
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.108-34C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.390-34C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.284-34C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.390-34C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-16404C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.192-34C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.441-34C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.390-34C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.192-34C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429524
  ensembl transcript: ENST00000521544
  gene symbol: NDRG1
  hgvsc: ENST00000521544.1:c.390-34C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.390-34C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429840
  ensembl transcript: ENST00000520943
  gene symbol: NDRG1
  hgvsc: ENST00000520943.1:c.423-34C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.390-34C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.215-69C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.526+708C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-11797C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.390-34C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.147-34C>T
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20083
  bin: 7.5e0
  variant carriers: 190
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 6.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1906
  bin: 2.25e1
  variant carriers: 94
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 3.25e1
  variant carriers: 15
genotype quality: GenotypeQuality
num of homozygotes: 36
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff

8-134270714-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134270714
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134270714
    reference: chr 8
allele count: 4
allele frequency: 6.756300249983109e-5
allele num: 59204
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.108-45G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.441-45G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429524
  ensembl transcript: ENST00000521544
  gene symbol: NDRG1
  hgvsc: ENST00000521544.1:c.390-45G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.390-45G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-16415G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.192-45G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.390-45G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.390-45G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.147-45G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.284-45G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.192-45G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.526+697G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.390-45G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-11808G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.390-45G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429840
  ensembl transcript: ENST00000520943
  gene symbol: NDRG1
  hgvsc: ENST00000520943.1:c.423-45G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.215-80G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.390-45G>A
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6550
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

8-134270716-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134270716
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134270716
    reference: chr 8
allele count: 1
allele frequency: 1.701548409052238e-5
allele num: 58770
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.390-47C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.390-47C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429524
  ensembl transcript: ENST00000521544
  gene symbol: NDRG1
  hgvsc: ENST00000521544.1:c.390-47C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.390-47C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.192-47C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.108-47C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.441-47C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.390-47C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-16417C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.390-47C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.526+695C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.390-47C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429840
  ensembl transcript: ENST00000520943
  gene symbol: NDRG1
  hgvsc: ENST00000520943.1:c.423-47C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.215-82C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.192-47C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.284-47C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-11810C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.147-47C>G
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

8-134271361-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134271361
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134271361
    reference: chr 8
allele count: 2
allele frequency: 1.648070932972955e-5
allele num: 121354
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.389+50C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.389+50C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.191+50C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429524
  ensembl transcript: ENST00000521544
  gene symbol: NDRG1
  hgvsc: ENST00000521544.1:c.389+50C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.389+50C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.389+50C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.440+50C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429840
  ensembl transcript: ENST00000520943
  gene symbol: NDRG1
  hgvsc: ENST00000520943.1:c.422+50C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.526+50C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518094
  gene symbol: NDRG1
  hgvsc: ENST00000518094.1:n.324C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.283+50C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517745
  gene symbol: NDRG1
  hgvsc: ENST00000517745.1:n.269C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.107+50C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.191+50C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-12455C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-17062C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.146+50C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.215-727C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.389+50C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.389+50C>A
  variant of: http://identifiers.org/hgnc/7679
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2985
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: MQ
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

8-134271370-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134271370
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134271370
    reference: chr 8
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.283+41G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-17071G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.526+41G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.389+41G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429840
  ensembl transcript: ENST00000520943
  gene symbol: NDRG1
  hgvsc: ENST00000520943.1:c.422+41G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.440+41G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.389+41G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.389+41G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517745
  gene symbol: NDRG1
  hgvsc: ENST00000517745.1:n.260G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.389+41G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.146+41G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.389+41G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.107+41G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518094
  gene symbol: NDRG1
  hgvsc: ENST00000518094.1:n.315G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429524
  ensembl transcript: ENST00000521544
  gene symbol: NDRG1
  hgvsc: ENST00000521544.1:c.389+41G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.191+41G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-12464G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.389+41G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.215-736G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.191+41G>A
  variant of: http://identifiers.org/hgnc/7679
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4803
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/8-134271378-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134271378
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134271378
    reference: chr 8
allele count: 3
allele frequency: 2.472147142197904e-5
allele num: 121352
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517745
  gene symbol: NDRG1
  hgvsc: ENST00000517745.1:n.252G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.389+33G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.440+33G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518094
  gene symbol: NDRG1
  hgvsc: ENST00000518094.1:n.307G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.389+33G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.146+33G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.191+33G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.215-744G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.389+33G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.526+33G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.283+33G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.107+33G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-17079G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429840
  ensembl transcript: ENST00000520943
  gene symbol: NDRG1
  hgvsc: ENST00000520943.1:c.422+33G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.389+33G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429524
  ensembl transcript: ENST00000521544
  gene symbol: NDRG1
  hgvsc: ENST00000521544.1:c.389+33G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-12472G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.389+33G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.191+33G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.389+33G>T
  variant of: http://identifiers.org/hgnc/7679
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4386
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum

8-134271392-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134271392
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134271392
    reference: chr 8
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517745
  gene symbol: NDRG1
  hgvsc: ENST00000517745.1:n.238C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.389+19C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429524
  ensembl transcript: ENST00000521544
  gene symbol: NDRG1
  hgvsc: ENST00000521544.1:c.389+19C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.389+19C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.389+19C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.389+19C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-17093C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429840
  ensembl transcript: ENST00000520943
  gene symbol: NDRG1
  hgvsc: ENST00000520943.1:c.422+19C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.191+19C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.389+19C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518094
  gene symbol: NDRG1
  hgvsc: ENST00000518094.1:n.293C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.107+19C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.215-758C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.191+19C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.440+19C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-12486C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.283+19C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.389+19C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.526+19C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.146+19C>T
  variant of: http://identifiers.org/hgnc/7679
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

8-134271393-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134271393
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134271393
    reference: chr 8
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.107+18G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429840
  ensembl transcript: ENST00000520943
  gene symbol: NDRG1
  hgvsc: ENST00000520943.1:c.422+18G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.389+18G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518094
  gene symbol: NDRG1
  hgvsc: ENST00000518094.1:n.292G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429524
  ensembl transcript: ENST00000521544
  gene symbol: NDRG1
  hgvsc: ENST00000521544.1:c.389+18G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.526+18G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.389+18G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.191+18G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517745
  gene symbol: NDRG1
  hgvsc: ENST00000517745.1:n.237G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.283+18G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.440+18G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.389+18G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.389+18G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.146+18G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-17094G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.191+18G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.389+18G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.215-759G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-12487G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.389+18G>A
  variant of: http://identifiers.org/hgnc/7679
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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: C
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

8-134271398-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134271398
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134271398
    reference: chr 8
allele count: 12
allele frequency: 9.888099672044694e-5
allele num: 121358
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429524
  ensembl transcript: ENST00000521544
  gene symbol: NDRG1
  hgvsc: ENST00000521544.1:c.389+13G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-12492G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-17099G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.440+13G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517745
  gene symbol: NDRG1
  hgvsc: ENST00000517745.1:n.232G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.191+13G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.389+13G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.283+13G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518094
  gene symbol: NDRG1
  hgvsc: ENST00000518094.1:n.287G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.389+13G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.389+13G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.389+13G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.526+13G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.146+13G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.389+13G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.107+13G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.215-764G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429840
  ensembl transcript: ENST00000520943
  gene symbol: NDRG1
  hgvsc: ENST00000520943.1:c.422+13G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.191+13G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.389+13G>C
  variant of: http://identifiers.org/hgnc/7679
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: African
population: South Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ

8-134271402-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134271402
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134271402
    reference: chr 8
allele count: 2
allele frequency: 1.648016612007449e-5
allele num: 121358
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.389+9G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.389+9G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429840
  ensembl transcript: ENST00000520943
  gene symbol: NDRG1
  hgvsc: ENST00000520943.1:c.422+9G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.440+9G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.389+9G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.283+9G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518094
  gene symbol: NDRG1
  hgvsc: ENST00000518094.1:n.283G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.389+9G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.389+9G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-17103G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-12496G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517745
  gene symbol: NDRG1
  hgvsc: ENST00000517745.1:n.228G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.389+9G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.191+9G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.146+9G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429524
  ensembl transcript: ENST00000521544
  gene symbol: NDRG1
  hgvsc: ENST00000521544.1:c.389+9G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.526+9G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.107+9G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.215-768G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.191+9G>A
  variant of: http://identifiers.org/hgnc/7679
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3657
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

8-134271403-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134271403
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134271403
    reference: chr 8
allele count: 19
allele frequency: 1.565667386324307e-4
allele num: 121354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.37-17104C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.146+8C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518094
  gene symbol: NDRG1
  hgvsc: ENST00000518094.1:n.282C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.389+8C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.191+8C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.191+8C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517331
  gene symbol: NDRG1
  hgvsc: ENST00000517331.1:n.107+8C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.49-12497C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429380
  ensembl transcript: ENST00000522377
  gene symbol: NDRG1
  hgvsc: ENST00000522377.1:c.389+8C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.389+8C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.389+8C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.389+8C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000517745
  gene symbol: NDRG1
  hgvsc: ENST00000517745.1:n.227C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.283+8C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429524
  ensembl transcript: ENST00000521544
  gene symbol: NDRG1
  hgvsc: ENST00000521544.1:c.389+8C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429840
  ensembl transcript: ENST00000520943
  gene symbol: NDRG1
  hgvsc: ENST00000520943.1:c.422+8C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.440+8C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.526+8C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.215-769C>T
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
hgvs: c.389+8C>T
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 33
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 518
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 845
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 39
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4523
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 988
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 678
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2225
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 888
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41787
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8496
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9850
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6152
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11250
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.072574202666994e-5
allele num: 65092
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16012
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.973e1

FS
type: SiteQuality
SIO_000300: 6.69e-1

DP
type: SiteQuality
SIO_000300: 1.681745e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

QD
type: SiteQuality
SIO_000300: 1.227e1

MQRankSum
type: SiteQuality
SIO_000300: 8.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -5.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.28e0

GenotypeQuality
all individuals: 39
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4536
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41740
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 829
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 898
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6269
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 36
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 989
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 652
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 163
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 419
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11254
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16026
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.014816318246397e-4
allele num: 9854
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6156
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8496
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65144
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.476e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

VQSLOD
type: SiteQuality
SIO_000300: 1.77e0

MQ
type: SiteQuality
SIO_000300: 6.045e1

MQRankSum
type: SiteQuality
SIO_000300: -3.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.8e-2

QD
type: SiteQuality
SIO_000300: 1.355e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

DP
type: SiteQuality
SIO_000300: 1.682828e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.81e0

GenotypeQuality
all individuals: 165
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 997
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2124
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6267
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 621
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 907
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41898
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 804
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4570
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 251
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6166
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8498
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.880994671403197e-5
allele num: 11260
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16044
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65194
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.85e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

DP
type: SiteQuality
SIO_000300: 1.684634e6

QD
type: SiteQuality
SIO_000300: 1.475e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.546e0

VQSLOD
type: SiteQuality
SIO_000300: 7.39e-1

MQ
type: SiteQuality
SIO_000300: 5.951e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.068e0

GenotypeDepth
all individuals: 594
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6267
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 251
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1605
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4704
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 915
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 426
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 531
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 486
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1016
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42534
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9994
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.522394421946838e-5
allele num: 65686
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11326
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16150
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6284
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.705597e6

VQSLOD
type: SiteQuality
SIO_000300: -1.735e0

MQ
type: SiteQuality
SIO_000300: 5.889e1

MQRankSum
type: SiteQuality
SIO_000300: -7.97e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.268e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 7.82e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.14e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.97e-1

GenotypeDepth
all individuals: 2509
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43075
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1536
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4749
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 481
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6280
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 171
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1023
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 933
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 1.994017946161515e-4
allele num: 10030
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11334
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.041732570872369e-5
allele num: 65752
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16170
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16795141322121e-4
allele num: 8562
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.362e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.0e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.63e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.37e0

QD
type: SiteQuality
SIO_000300: 1.218e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -5.69e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.45e-1

DP
type: SiteQuality
SIO_000300: 1.707927e6

GenotypeDepth
all individuals: 308
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 290
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1536
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1023
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 933
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43075
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4749
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6280
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 257
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 481
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 7.604331427180922e-5
allele num: 65752
num of homozygotes: 0

East Asian
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African
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ClippingRankSum
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InbreedingCoeff
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FS
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MQ
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MQRankSum
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DP
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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QD
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SIO_000300: 1.218e1

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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European (Finnish)
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Other
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Latino
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East Asian
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South Asian
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FS
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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QD
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VQSLOD
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ClippingRankSum
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MQ
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 0
allele frequency: 0.0e0
allele num: 6358
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.51437138443832e-5
allele num: 66034
num of homozygotes: 0

East Asian
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South Asian
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ClippingRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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FS
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MQ
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DP
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QD
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GenotypeDepth
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variant carriers: 39

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 3
allele frequency: 1.848201084277969e-4
allele num: 16232
num of homozygotes: 0

European (Non-Finnish)
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allele count: 7
allele frequency: 1.059514439668221e-4
allele num: 66068
num of homozygotes: 0

Latino
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allele count: 7
allele frequency: 6.128523901243215e-4
allele num: 11422
num of homozygotes: 0

European (Finnish)
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allele count: 3
allele frequency: 4.714016341923319e-4
allele num: 6364
num of homozygotes: 0

East Asian
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allele count: 0
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Other
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allele count: 2
allele frequency: 2.304147465437788e-3
allele num: 868
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African
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allele frequency: 4.108648754657776e-2
allele num: 10198
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.6e-2

BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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QD
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MQRankSum
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VQSLOD
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FS
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SIO_000300: 5.27e-1

MQ
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SIO_000300: 5.973e1

DP
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SIO_000300: 1.736806e6

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1.160900859066636e-4
allele num: 8614
num of homozygotes: 0

European (Non-Finnish)
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Latino
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South Asian
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African
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Other
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European (Finnish)
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BaseQRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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MQRankSum
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FS
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ReadPosRankSum
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QD
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DP
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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European (Finnish)
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Other
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East Asian
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European (Non-Finnish)
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QD
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ClippingRankSum
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MQRankSum
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MQ
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DP
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FS
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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European (Non-Finnish)
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Other
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African
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South Asian
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MQRankSum
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MQ
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FS
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DP
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QD
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 9.869719699960521e-5
allele num: 10132
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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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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ReadPosRankSum
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SIO_000300: -2.49e-1

QD
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MQ
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ClippingRankSum
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VQSLOD
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FS
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InbreedingCoeff
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BaseQRankSum
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DP
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10120
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.521005080156968e-5
allele num: 65746
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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Other
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MQRankSum
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QD
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MQ
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ReadPosRankSum
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FS
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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DP
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.521421616358325e-5
allele num: 65728
num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
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InbreedingCoeff
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SIO_000300: -3.0e-4

BaseQRankSum
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SIO_000300: -2.344e0

ClippingRankSum
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SIO_000300: -1.604e0

QD
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VQSLOD
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MQ
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SIO_000300: 6.0e1

DP
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FS
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SIO_000300: 0.0e0

ReadPosRankSum
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SIO_000300: 1.26e0

MQRankSum
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SIO_000300: 6.17e-1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 0
allele frequency: 0.0e0
allele num: 6292
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 3
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allele num: 65558
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East Asian
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South Asian
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DP
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VQSLOD
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MQ
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ReadPosRankSum
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BaseQRankSum
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QD
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MQRankSum
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InbreedingCoeff
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FS
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ClippingRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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South Asian
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African
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East Asian
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European (Finnish)
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European (Non-Finnish)
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VQSLOD
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MQ
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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FS
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ClippingRankSum
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QD
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DP
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GenotypeDepth
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variant carriers: 1

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

Latino
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allele count: 1
allele frequency: 9.05961224859576e-5
allele num: 11038
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63952
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8318
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15630
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.875e0

BaseQRankSum
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SIO_000300: 1.76e-1

MQ
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SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 7.99e-1

ReadPosRankSum
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SIO_000300: 3.93e-1

QD
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SIO_000300: 5.01e0

DP
type: SiteQuality
SIO_000300: 1.646343e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.28e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
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variant carriers: 0

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

Other
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allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

Latino
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allele count: 2
allele frequency: 1.814552712756306e-4
allele num: 11022
num of homozygotes: 0

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

East Asian
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: 9750
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63888
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
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SIO_000300: 1.88e0

MQ
type: SiteQuality
SIO_000300: 5.94e1

DP
type: SiteQuality
SIO_000300: 1.640323e6

InbreedingCoeff
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QD
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SIO_000300: 1.202e1

VQSLOD
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SIO_000300: 3.23e-1

FS
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SIO_000300: 7.19e0

ReadPosRankSum
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SIO_000300: 1.14e0

ClippingRankSum
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SIO_000300: 1.48e0

MQRankSum
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SIO_000300: 3.76e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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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: 3
allele frequency: 1.93050193050193e-4
allele num: 15540
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9690
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6046
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10946
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63584
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8250
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MQRankSum
type: SiteQuality
SIO_000300: 1.54e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

QD
type: SiteQuality
SIO_000300: 1.227e1

DP
type: SiteQuality
SIO_000300: 1.625886e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.48e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

VQSLOD
type: SiteQuality
SIO_000300: -2.094e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.8e-1

GenotypeDepth
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bin: 6.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 5998
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.580378026423921e-5
allele num: 63276
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8198
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10888
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
SIO_000300: -1.985e0

FS
type: SiteQuality
SIO_000300: 1.2799e1

DP
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SIO_000300: 1.61269e6

ClippingRankSum
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BaseQRankSum
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SIO_000300: 2.15e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.7e-2

QD
type: SiteQuality
SIO_000300: 1.392e1

MQ
type: SiteQuality
SIO_000300: 5.873e1

MQRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 5974
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
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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

South Asian
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allele count: 1
allele frequency: 6.507874528179097e-5
allele num: 15366
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 62900
num of homozygotes: 0

Other
type: Population
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ReadPosRankSum
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SIO_000300: -5.669999999999999e-1

ClippingRankSum
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InbreedingCoeff
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MQRankSum
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QD
type: SiteQuality
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BaseQRankSum
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SIO_000300: -2.65e-1

FS
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MQ
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DP
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VQSLOD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5948
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
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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: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.597750367482585e-5
allele num: 62588
num of homozygotes: 0

DP
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SIO_000300: 1.579158e6

MQ
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MQRankSum
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VQSLOD
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SIO_000300: -2.802e0

FS
type: SiteQuality
SIO_000300: 2.473e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.82e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

QD
type: SiteQuality
SIO_000300: 8.220000000000001e0

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.599897606553181e-5
allele num: 62504
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9516
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5936
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 6.56e0

ReadPosRankSum
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SIO_000300: -2.31e-1

MQ
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SIO_000300: 5.895e1

MQRankSum
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BaseQRankSum
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SIO_000300: 6.26e-1

VQSLOD
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DP
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QD
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InbreedingCoeff
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SIO_000300: -1.1e-3

ClippingRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 802
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variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 59246
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9860
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.799020940984498e-5
allele num: 14708
num of homozygotes: 0

East Asian
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
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num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5632
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.596e0

VQSLOD
type: SiteQuality
SIO_000300: 4.83e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.95e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.7e-2

MQ
type: SiteQuality
SIO_000300: 5.95e1

FS
type: SiteQuality
SIO_000300: 2.63e0

QD
type: SiteQuality
SIO_000300: 9.41e0

DP
type: SiteQuality
SIO_000300: 1.338324e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14510
num of homozygotes: 0

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

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
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num of homozygotes: 0

Latino
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allele count: 2
allele frequency: 2.072538860103627e-4
allele num: 9650
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58368
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.05e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.44e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.35e-1

VQSLOD
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ClippingRankSum
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InbreedingCoeff
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SIO_000300: -3.0e-3

MQ
type: SiteQuality
SIO_000300: 6.093e1

QD
type: SiteQuality
SIO_000300: 9.970000000000001e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.297559e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.562011871290222e-4
allele num: 6402
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8042
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Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

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

InbreedingCoeff
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SIO_000300: -6.5e-3

ClippingRankSum
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BaseQRankSum
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FS
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VQSLOD
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QD
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MQRankSum
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MQ
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ReadPosRankSum
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DP
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GenotypeDepth
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variant carriers: 1

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

European (Non-Finnish)
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allele count: 0
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South Asian
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allele frequency: 1.019084676672225e-3
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African
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

ClippingRankSum
type: SiteQuality
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DP
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SIO_000300: 1.197921e6

InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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FS
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MQRankSum
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VQSLOD
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MQ
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

Latino
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allele frequency: 2.126754572522331e-4
allele num: 4702
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele frequency: 5.837370848169984e-5
allele num: 34262
num of homozygotes: 0

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

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

East Asian
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allele frequency: 0.0e0
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VQSLOD
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FS
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MQ
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QD
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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DP
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SIO_000300: 1.244706e6

BaseQRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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allele frequency: 0.0e0
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European (Finnish)
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South Asian
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Latino
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East Asian
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European (Non-Finnish)
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VQSLOD
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BaseQRankSum
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MQRankSum
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FS
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DP
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MQ
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InbreedingCoeff
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ClippingRankSum
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QD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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Other
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European (Finnish)
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Latino
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East Asian
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South Asian
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MQRankSum
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FS
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QD
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ClippingRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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DP
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GenotypeDepth
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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 (Non-Finnish)
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European (Finnish)
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Latino
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MQ
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FS
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DP
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ClippingRankSum
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MQRankSum
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4410
num of homozygotes: 0

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

East Asian
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allele count: 1
allele frequency: 1.464557703573521e-4
allele num: 6828
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 49220
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.158e0

QD
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SIO_000300: 8.529999999999999e0

ReadPosRankSum
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SIO_000300: -1.208e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.68e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.969e-1

MQRankSum
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SIO_000300: 5.78e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

DP
type: SiteQuality
SIO_000300: 1.495054e6

GenotypeDepth
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bin: 7.5e0
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6838
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8294
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4420
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 7.855459544383346e-5
allele num: 12730
num of homozygotes: 0

African
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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: 664
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 49316
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.498082e6

FS
type: SiteQuality
SIO_000300: 1.447e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

MQRankSum
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MQ
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BaseQRankSum
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VQSLOD
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QD
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SIO_000300: 8.710000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.64e-1

GenotypeDepth
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bin: 5.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 339
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8328
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.258178158027177e-4
allele num: 7948
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6852
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 664
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.019386106623587e-5
allele num: 49520
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 12738
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4444
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

DP
type: SiteQuality
SIO_000300: 1.500483e6

FS
type: SiteQuality
SIO_000300: 4.145e0

QD
type: SiteQuality
SIO_000300: 1.342e1

ReadPosRankSum
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SIO_000300: 7.17e-1

MQRankSum
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SIO_000300: -1.214e0

VQSLOD
type: SiteQuality
SIO_000300: 1.17e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.7e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.12e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2.006098539560263e-5
allele num: 49848
num of homozygotes: 0

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6890
num of homozygotes: 0

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

InbreedingCoeff
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SIO_000300: -2.2e-3

VQSLOD
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MQ
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FS
type: SiteQuality
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DP
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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QD
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BaseQRankSum
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SIO_000300: -1.001e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4474
num of homozygotes: 0

Other
type: Population
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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
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num of homozygotes: 0

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

African
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 12762
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European (Non-Finnish)
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allele count: 1
allele frequency: 2.007790226077179e-5
allele num: 49806
num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4498
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.400504181505342e-4
allele num: 49982
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8390
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.703e0

DP
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MQRankSum
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MQ
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InbreedingCoeff
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ClippingRankSum
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QD
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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European (Non-Finnish)
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European (Finnish)
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Other
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BaseQRankSum
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MQ
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MQRankSum
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DP
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InbreedingCoeff
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VQSLOD
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FS
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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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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South Asian
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Latino
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Other
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European (Non-Finnish)
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East Asian
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VQSLOD
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MQRankSum
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DP
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ReadPosRankSum
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FS
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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QD
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Non-Finnish)
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Latino
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Other
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African
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South Asian
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MQ
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FS
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DP
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QD
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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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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European (Finnish)
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African
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European (Non-Finnish)
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East Asian
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Other
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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QD
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MQ
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VQSLOD
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DP
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European (Finnish)
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African
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European (Non-Finnish)
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East Asian
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Latino
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DP
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VQSLOD
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MQRankSum
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FS
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MQ
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QD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

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

South Asian
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allele frequency: 8.204791598293403e-5
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 45302
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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Latino
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MQRankSum
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VQSLOD
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MQ
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BaseQRankSum
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FS
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ClippingRankSum
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QD
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DP
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e0

InbreedingCoeff
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SIO_000300: -4.3e-3

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1
allele frequency: 1.319609395618897e-4
allele num: 7578
num of homozygotes: 0

Latino
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allele count: 4
allele frequency: 5.492996429552321e-4
allele num: 7282
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

East Asian
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allele count: 1
allele frequency: 1.559575795383656e-4
allele num: 6412
num of homozygotes: 0

Other
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allele count: 1
allele frequency: 1.602564102564103e-3
allele num: 624
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3856
num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 8.888098835659053e-5
allele num: 45004
num of homozygotes: 0

DP
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SIO_000300: 1.34824e6

MQ
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VQSLOD
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BaseQRankSum
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MQRankSum
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QD
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FS
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SIO_000300: 2.629e0

InbreedingCoeff
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SIO_000300: -4.8e-3

ReadPosRankSum
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SIO_000300: 1.46e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.19e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 6534
num of homozygotes: 0

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

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

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 592
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.40940632228219e-5
allele num: 41504
num of homozygotes: 0

MQRankSum
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SIO_000300: -4.23e-1

ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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FS
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QD
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DP
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SIO_000300: 1.238432e6

MQ
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SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.40016802016242e-4
allele num: 7142
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41042
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 6478
num of homozygotes: 0

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

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

Other
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allele count: 0
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FS
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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QD
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MQRankSum
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MQ
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.469623629358886e-5
allele num: 40492
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
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South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5866
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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FS
type: SiteQuality
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VQSLOD
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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DP
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MQ
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ReadPosRankSum
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InbreedingCoeff
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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Latino
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East Asian
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South Asian
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European (Non-Finnish)
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Other
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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DP
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FS
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VQSLOD
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MQ
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BaseQRankSum
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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European (Non-Finnish)
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Latino
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Other
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European (Finnish)
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ClippingRankSum
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DP
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InbreedingCoeff
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MQ
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BaseQRankSum
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FS
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VQSLOD
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ReadPosRankSum
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QD
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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European (Finnish)
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European (Non-Finnish)
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allele num: 36050
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African
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allele frequency: 1.202153110047847e-1
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Other
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Latino
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allele frequency: 6.622516556291391e-3
allele num: 5436
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BaseQRankSum
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SIO_000300: -3.69e-1

DP
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SIO_000300: 1.154084e6

MQ
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ReadPosRankSum
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FS
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VQSLOD
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MQRankSum
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ClippingRankSum
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QD
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InbreedingCoeff
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SIO_000300: 2.24e-2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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East Asian
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European (Non-Finnish)
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South Asian
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European (Finnish)
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Latino
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ClippingRankSum
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MQRankSum
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VQSLOD
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QD
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FS
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MQ
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InbreedingCoeff
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BaseQRankSum
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DP
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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Other
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South Asian
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Latino
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European (Finnish)
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MQRankSum
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QD
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FS
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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MQ
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DP
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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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European (Non-Finnish)
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Latino
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African
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European (Finnish)
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East Asian
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Other
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South Asian
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MQ
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QD
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FS
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MQRankSum
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DP
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Finnish)
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East Asian
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European (Non-Finnish)
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South Asian
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QD
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VQSLOD
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FS
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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DP
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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East Asian
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European (Finnish)
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European (Non-Finnish)
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African
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MQ
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MQRankSum
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ReadPosRankSum
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QD
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InbreedingCoeff
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VQSLOD
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FS
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DP
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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East Asian
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African
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European (Non-Finnish)
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InbreedingCoeff
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FS
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VQSLOD
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MQ
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ClippingRankSum
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ReadPosRankSum
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DP
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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East Asian
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African
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European (Non-Finnish)
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DP
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VQSLOD
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ClippingRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Non-Finnish)
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European (Finnish)
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East Asian
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African
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South Asian
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QD
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InbreedingCoeff
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MQRankSum
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DP
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ReadPosRankSum
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VQSLOD
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FS
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MQ
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bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8999
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 3055
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5180
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3917
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2611
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 905
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2981
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4386
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5350
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2128
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 73
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1834
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4749
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4803
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 46
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3978
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48368
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1712
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3036
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1633
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 860
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2175
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1608
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 36
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1135
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 1.923816852635629e-4
allele num: 10396
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: 906
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
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: 66700
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.413e0

QD
type: SiteQuality
SIO_000300: 1.087e1

DP
type: SiteQuality
SIO_000300: 3.989101e6

VQSLOD
type: SiteQuality
SIO_000300: 3.38e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.942e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.44e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e0

MQ
type: SiteQuality
SIO_000300: 5.918e1

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000104419
ensembl protein: ENSP00000429272
ensembl transcript: ENST00000519580
gene symbol: NDRG1
hgvsc: ENST00000519580.1:c.389+8C>T
variant of: http://identifiers.org/hgnc/7679

GenotypeDepth
all individuals: 5181
bin: 5.25e1
variant carriers: 0