8-134276925-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134276925
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134276925
    reference: chr 8
allele count: 1
allele frequency: 8.242120532770671e-6
allele num: 121328
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000523931
  gene symbol: NDRG1
  hgvsc: ENST00000523931.1:n.311A>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.100-30A>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.151-30A>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.100-30A>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.-38-2515A>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.237-30A>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.100-2515A>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.-99-30A>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-99-30A>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.100-30A>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.100-30A>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.36+19594A>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.49-18019A>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.100-30A>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.100-30A>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.133-30A>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.100-30A>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.262-30A>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.-99-30A>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.100-30A>T
  variant of: http://identifiers.org/hgnc/7679
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP

8-134276928-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134276928
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134276928
    reference: chr 8
allele count: 1
allele frequency: 8.242528148233626e-6
allele num: 121322
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.100-33A>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.100-33A>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.100-33A>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.133-33A>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.100-2518A>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.-99-33A>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.100-33A>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.237-33A>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.100-33A>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.-38-2518A>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: ENST00000523931
  gene symbol: NDRG1
  hgvsc: ENST00000523931.1:n.308A>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.36+19591A>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.100-33A>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.-99-33A>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.151-33A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.262-33A>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.100-33A>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.100-33A>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.49-18022A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-99-33A>G
  variant of: http://identifiers.org/hgnc/7679
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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: T
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD

8-134276930-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134276930
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134276930
    reference: chr 8
allele count: 1
allele frequency: 8.243615319934711e-6
allele num: 121306
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.100-35A>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.100-35A>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.100-35A>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.100-35A>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.100-35A>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.100-35A>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.151-35A>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.100-35A>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.-99-35A>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.49-18024A>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: ENST00000523931
  gene symbol: NDRG1
  hgvsc: ENST00000523931.1:n.306A>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.262-35A>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.36+19589A>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.133-35A>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.-38-2520A>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-99-35A>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.-99-35A>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.237-35A>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.100-35A>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.100-2520A>C
  variant of: http://identifiers.org/hgnc/7679
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-134276930-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134276930
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134276929
    reference: chr 8
allele count: 1
allele frequency: 8.243615319934711e-6
allele num: 121306
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.100-36delC
  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: ENST00000523931
  gene symbol: NDRG1
  hgvsc: ENST00000523931.1:n.305delC
  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.100-36delC
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-99-36delC
  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.-38-2521delC
  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.100-36delC
  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.151-36delC
  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.100-36delC
  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.100-36delC
  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.237-36delC
  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.49-18025delC
  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.-99-36delC
  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.100-2521delC
  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.100-36delC
  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.100-36delC
  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.100-36delC
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.262-36delC
  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.133-36delC
  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.-99-36delC
  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.36+19588delC
  variant of: http://identifiers.org/hgnc/7679
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
reference allele: TG
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

8-134276934-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134276934
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134276934
    reference: chr 8
allele count: 1
allele frequency: 8.245926512302922e-6
allele num: 121272
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.100-39C>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: ENST00000523931
  gene symbol: NDRG1
  hgvsc: ENST00000523931.1:n.302C>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.49-18028C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.262-39C>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.100-39C>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.100-39C>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-99-39C>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.133-39C>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.100-2524C>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.-99-39C>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.-38-2524C>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.100-39C>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.151-39C>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.100-39C>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.237-39C>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.36+19585C>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.100-39C>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.100-39C>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.100-39C>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.-99-39C>A
  variant of: http://identifiers.org/hgnc/7679
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6408
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

8-134276935-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134276935
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134276935
    reference: chr 8
allele count: 1386
allele frequency: 1.142866566617742e-2
allele num: 121274
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-99-40A>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.100-40A>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.100-2525A>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.-99-40A>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.100-40A>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: ENST00000523931
  gene symbol: NDRG1
  hgvsc: ENST00000523931.1:n.301A>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.100-40A>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.49-18029A>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.100-40A>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.36+19584A>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.100-40A>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.151-40A>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.133-40A>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.100-40A>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.100-40A>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.237-40A>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.-99-40A>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.100-40A>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.-38-2525A>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.262-40A>T
  variant of: http://identifiers.org/hgnc/7679
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6387
  bin: 3.75e1
  variant carriers: 165
genotype quality: GenotypeQuality
num of homozygotes: 14
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum

8-134276939-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134276939
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134276939
    reference: chr 8
allele count: 4
allele frequency: 3.299132328197684e-5
allele num: 121244
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.49-18033A>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.36+19580A>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.100-2529A>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.237-44A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-99-44A>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.-99-44A>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.100-44A>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.100-44A>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.100-44A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.262-44A>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: ENST00000523931
  gene symbol: NDRG1
  hgvsc: ENST00000523931.1:n.297A>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.151-44A>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.100-44A>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.133-44A>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.-99-44A>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.100-44A>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.-38-2529A>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.100-44A>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.100-44A>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.100-44A>G
  variant of: http://identifiers.org/hgnc/7679
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1326
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: African
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS

8-134276940-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134276940
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134276940
    reference: chr 8
allele count: 1
allele frequency: 8.250688932525866e-6
allele num: 121202
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.133-45C>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.100-2530C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.262-45C>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: ENST00000523931
  gene symbol: NDRG1
  hgvsc: ENST00000523931.1:n.296C>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.100-45C>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.-99-45C>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.49-18034C>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.100-45C>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.100-45C>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.36+19579C>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.100-45C>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.-38-2530C>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.100-45C>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.237-45C>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.151-45C>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.100-45C>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.-99-45C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-99-45C>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.100-45C>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.100-45C>T
  variant of: http://identifiers.org/hgnc/7679
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3664
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

8-134276943-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134276943
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134276943
    reference: chr 8
allele count: 1
allele frequency: 8.253140319891718e-6
allele num: 121166
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429524
  ensembl transcript: ENST00000521544
  gene symbol: NDRG1
  hgvsc: ENST00000521544.1:c.100-48T>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.49-18037T>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.-38-2533T>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: ENST00000523931
  gene symbol: NDRG1
  hgvsc: ENST00000523931.1:n.293T>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.100-48T>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.262-48T>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.100-2533T>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.36+19576T>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-99-48T>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.100-48T>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.100-48T>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.100-48T>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.-99-48T>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.237-48T>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.133-48T>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.100-48T>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.151-48T>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.100-48T>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.100-48T>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.-99-48T>A
  variant of: http://identifiers.org/hgnc/7679
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD

8-134276946-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134276946
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134276946
    reference: chr 8
allele count: 3
allele frequency: 2.479297862845242e-5
allele num: 121002
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.-99-51G>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.100-2536G>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.100-51G>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.237-51G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-99-51G>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.36+19573G>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.133-51G>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.100-51G>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.100-51G>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.100-51G>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.49-18040G>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.151-51G>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.100-51G>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.100-51G>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: ENST00000523931
  gene symbol: NDRG1
  hgvsc: ENST00000523931.1:n.290G>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.-99-51G>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.100-51G>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.-38-2536G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.262-51G>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.100-51G>A
  variant of: http://identifiers.org/hgnc/7679
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11258
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP

8-134276947-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134276947
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134276947
    reference: chr 8
allele count: 5
allele frequency: 4.131275407343755e-5
allele num: 121028
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104419
  ensembl transcript: ENST00000523931
  gene symbol: NDRG1
  hgvsc: ENST00000523931.1:n.289C>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.-38-2537C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.262-52C>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.-99-52C>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.151-52C>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.100-52C>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.100-52C>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.133-52C>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.237-52C>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.36+19572C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-99-52C>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.100-52C>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.100-2537C>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.-99-52C>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.100-52C>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.49-18041C>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.100-52C>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.100-52C>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.100-52C>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.100-52C>T
  variant of: http://identifiers.org/hgnc/7679
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11121
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

8-134292425-AAG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134292425
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134292423
    reference: chr 8
allele count: 1
allele frequency: 8.319605983460623e-6
allele num: 120198
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.150+48_150+49delCT
  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.99+48_99+49delCT
  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.99+48_99+49delCT
  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.132+48_132+49delCT
  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.99+48_99+49delCT
  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.99+48_99+49delCT
  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.-100+48_-100+49delCT
  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.99+48_99+49delCT
  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.-39+48_-39+49delCT
  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.99+48_99+49delCT
  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.236+48_236+49delCT
  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.-99-15532_-99-15531delCT
  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.99+48_99+49delCT
  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.99+48_99+49delCT
  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.48+4080_48+4081delCT
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.261+48_261+49delCT
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-100+48_-100+49delCT
  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.36+4092_36+4093delCT
  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.99+48_99+49delCT
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11938
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6898
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: European (Finnish)
reference allele: AAG
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum

8-134292434-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134292434
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134292434
    reference: chr 8
allele count: 5
allele frequency: 4.15468731823243e-5
allele num: 120346
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.99+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.-100+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.36+4085G>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.99+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.99+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.48+4073G>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.99+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.-39+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.132+41G>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.-99-15539G>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.99+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: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.236+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: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.99+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.150+41G>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.99+41G>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.99+41G>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.99+41G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-100+41G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.261+41G>A
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15972
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

8-134292435-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134292435
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134292435
    reference: chr 8
allele count: 8
allele frequency: 6.641208699983397e-5
allele num: 120460
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.99+40C>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.99+40C>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.36+4084C>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.99+40C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-100+40C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.261+40C>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.99+40C>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.-39+40C>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.99+40C>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.132+40C>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.99+40C>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.-100+40C>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.99+40C>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.150+40C>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.99+40C>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.236+40C>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.48+4072C>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.-99-15540C>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.99+40C>T
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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: BaseQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS

8-134292442-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134292442
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134292442
    reference: chr 8
allele count: 174
allele frequency: 1.440397350993378e-3
allele num: 120800
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.132+33C>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.99+33C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-100+33C>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.236+33C>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.36+4077C>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.-99-15547C>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.-39+33C>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.99+33C>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.99+33C>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.-100+33C>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.150+33C>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.99+33C>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.99+33C>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.99+33C>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.99+33C>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.48+4065C>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.99+33C>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.99+33C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.261+33C>T
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2464
  bin: 9.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 5.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
num of homozygotes: 1
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

8-134292452-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134292452
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134292452
    reference: chr 8
allele count: 1
allele frequency: 8.258593066085262e-6
allele num: 121086
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.99+23C>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.99+23C>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.-100+23C>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.36+4067C>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.132+23C>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.99+23C>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.150+23C>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.99+23C>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.-39+23C>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.48+4055C>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.99+23C>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.99+23C>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.236+23C>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.-99-15557C>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.99+23C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-100+23C>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.99+23C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.261+23C>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.99+23C>T
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17096
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

8-134292455-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134292455
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134292455
    reference: chr 8
allele count: 1
allele frequency: 8.251642076773278e-6
allele num: 121188
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.-100+20T>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.-39+20T>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.99+20T>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.99+20T>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.99+20T>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.48+4052T>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.99+20T>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.236+20T>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.-99-15560T>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.99+20T>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.99+20T>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.132+20T>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.150+20T>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.99+20T>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.36+4064T>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.99+20T>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.99+20T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-100+20T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.261+20T>C
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17102
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

8-134292476-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134292476
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134292476
    reference: chr 8
allele count: 1
allele frequency: 8.241848811525402e-6
allele num: 121332
alternate allele: C
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.98A>G
  hgvsp: ENSP00000429272.1:p.Gln33Arg
  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: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.98A>G
  hgvsp: ENSP00000429172.1:p.Gln33Arg
  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.149A>G
  hgvsp: ENSP00000428345.1:p.Gln50Arg
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429840
  ensembl transcript: ENST00000520943
  gene symbol: NDRG1
  hgvsc: ENST00000520943.1:c.131A>G
  hgvsp: ENSP00000429840.1:p.Gln44Arg
  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.98A>G
  hgvsp: ENSP00000319977.7:p.Gln33Arg
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429524
  ensembl transcript: ENST00000521544
  gene symbol: NDRG1
  hgvsc: ENST00000521544.1:c.98A>G
  hgvsp: ENSP00000429524.1:p.Gln33Arg
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.260A>G
  hgvsp: ENSP00000428991.1:p.Gln87Arg
  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.235A>G
  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.98A>G
  hgvsp: ENSP00000429994.1:p.Gln33Arg
  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.-99-15581A>G
  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.98A>G
  hgvsp: ENSP00000404854.2:p.Gln33Arg
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-101A>G
  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.98A>G
  hgvsp: ENSP00000429380.1:p.Gln33Arg
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.-101A>G
  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.98A>G
  hgvsp: ENSP00000428384.1:p.Gln33Arg
  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.98A>G
  hgvsp: ENSP00000347028.5:p.Gln33Arg
  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.36+4043A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.-40A>G
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gln33Arg
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: DP

8-134292480-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134292480
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134292480
    reference: chr 8
allele count: 1
allele frequency: 8.241577108195424e-6
allele num: 121336
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.94G>C
  hgvsp: ENSP00000429272.1:p.Val32Leu
  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.127G>C
  hgvsp: ENSP00000429840.1:p.Val43Leu
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.-44G>C
  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.94G>C
  hgvsp: ENSP00000429994.1:p.Val32Leu
  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.94G>C
  hgvsp: ENSP00000429380.1:p.Val32Leu
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-105G>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.94G>C
  hgvsp: ENSP00000404854.2:p.Val32Leu
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.-105G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.256G>C
  hgvsp: ENSP00000428991.1:p.Val86Leu
  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.145G>C
  hgvsp: ENSP00000428345.1:p.Val49Leu
  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.94G>C
  hgvsp: ENSP00000429524.1:p.Val32Leu
  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.94G>C
  hgvsp: ENSP00000347028.5:p.Val32Leu
  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.36+4039G>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.94G>C
  hgvsp: ENSP00000429172.1:p.Val32Leu
  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.94G>C
  hgvsp: ENSP00000319977.7:p.Val32Leu
  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.94G>C
  hgvsp: ENSP00000428384.1:p.Val32Leu
  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.231G>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.48+4027G>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.-99-15585G>C
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Val32Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum

8-134292481-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134292481
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134292481
    reference: chr 8
allele count: 2
allele frequency: 1.648315421639085e-5
allele num: 121336
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.144T>C
  hgvsp: ENST00000520230.1:c.144T>C(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.93T>C
  hgvsp: ENST00000414097.2:c.93T>C(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.93T>C
  hgvsp: ENST00000354944.5:c.93T>C(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.93T>C
  hgvsp: ENST00000323851.7:c.93T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.-45T>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: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.230T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.93T>C
  hgvsp: ENST00000517599.1:c.93T>C(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.93T>C
  hgvsp: ENST00000519228.1:c.93T>C(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.93T>C
  hgvsp: ENST00000522377.1:c.93T>C(p.%3D)
  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.93T>C
  hgvsp: ENST00000521544.1:c.93T>C(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.93T>C
  hgvsp: ENST00000519580.1:c.93T>C(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.93T>C
  hgvsp: ENST00000522890.1:c.93T>C(p.%3D)
  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.-99-15586T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.-106T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.255T>C
  hgvsp: ENST00000522738.1:c.255T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-106T>C
  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.126T>C
  hgvsp: ENST00000520943.1:c.126T>C(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.36+4038T>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.48+4026T>C
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asp31Asp
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/8-134292486-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134292486
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134292486
    reference: chr 8
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429840
  ensembl transcript: ENST00000520943
  gene symbol: NDRG1
  hgvsc: ENST00000520943.1:c.121T>G
  hgvsp: ENSP00000429840.1:p.Phe41Val
  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.48+4021T>G
  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.88T>G
  hgvsp: ENSP00000429272.1:p.Phe30Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-111T>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.88T>G
  hgvsp: ENSP00000428384.1:p.Phe30Val
  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.88T>G
  hgvsp: ENSP00000347028.5:p.Phe30Val
  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.139T>G
  hgvsp: ENSP00000428345.1:p.Phe47Val
  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.36+4033T>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.-99-15591T>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.-50T>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.88T>G
  hgvsp: ENSP00000429994.1:p.Phe30Val
  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.88T>G
  hgvsp: ENSP00000404854.2:p.Phe30Val
  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.88T>G
  hgvsp: ENSP00000319977.7:p.Phe30Val
  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.88T>G
  hgvsp: ENSP00000429380.1:p.Phe30Val
  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.88T>G
  hgvsp: ENSP00000429524.1:p.Phe30Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.88T>G
  hgvsp: ENSP00000429172.1:p.Phe30Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.250T>G
  hgvsp: ENSP00000428991.1:p.Phe84Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.-111T>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: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.225T>G
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Phe30Val
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

8-134292487-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134292487
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134292487
    reference: chr 8
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.48+4020G>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.87G>A
  hgvsp: ENST00000519228.1:c.87G>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.224G>A
  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.87G>A
  hgvsp: ENST00000522377.1:c.87G>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.138G>A
  hgvsp: ENST00000520230.1:c.138G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.249G>A
  hgvsp: ENST00000522738.1:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-112G>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.-99-15592G>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.87G>A
  hgvsp: ENST00000414097.2:c.87G>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.87G>A
  hgvsp: ENST00000519580.1:c.87G>A(p.%3D)
  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.87G>A
  hgvsp: ENST00000521544.1:c.87G>A(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.120G>A
  hgvsp: ENST00000520943.1:c.120G>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.36+4032G>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.87G>A
  hgvsp: ENST00000323851.7:c.87G>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.87G>A
  hgvsp: ENST00000354944.5:c.87G>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.87G>A
  hgvsp: ENST00000522890.1:c.87G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.-112G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.-51G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.87G>A
  hgvsp: ENST00000517599.1:c.87G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Glu29Glu
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

8-134292488-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134292488
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134292488
    reference: chr 8
allele count: 2
allele frequency: 1.648152421135907e-5
allele num: 121348
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.137A>C
  hgvsp: ENSP00000428345.1:p.Glu46Ala
  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.48+4019A>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.119A>C
  hgvsp: ENSP00000429840.1:p.Glu40Ala
  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.86A>C
  hgvsp: ENSP00000404854.2:p.Glu29Ala
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.-52A>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.248A>C
  hgvsp: ENSP00000428991.1:p.Glu83Ala
  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.86A>C
  hgvsp: ENSP00000429380.1:p.Glu29Ala
  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.86A>C
  hgvsp: ENSP00000429994.1:p.Glu29Ala
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-113A>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.-113A>C
  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.86A>C
  hgvsp: ENSP00000319977.7:p.Glu29Ala
  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.86A>C
  hgvsp: ENSP00000429272.1:p.Glu29Ala
  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.86A>C
  hgvsp: ENSP00000429524.1:p.Glu29Ala
  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.86A>C
  hgvsp: ENSP00000428384.1:p.Glu29Ala
  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.-99-15593A>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.36+4031A>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: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.223A>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.86A>C
  hgvsp: ENSP00000429172.1:p.Glu29Ala
  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.86A>C
  hgvsp: ENSP00000347028.5:p.Glu29Ala
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Glu29Ala
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

8-134292497-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134292497
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134292497
    reference: chr 8
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: G
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.77T>C
  hgvsp: ENSP00000429380.1:p.Leu26Pro
  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.110T>C
  hgvsp: ENSP00000429840.1:p.Leu37Pro
  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.128T>C
  hgvsp: ENSP00000428345.1:p.Leu43Pro
  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.36+4022T>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.-99-15602T>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: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.214T>C
  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.77T>C
  hgvsp: ENSP00000429994.1:p.Leu26Pro
  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.77T>C
  hgvsp: ENSP00000429272.1:p.Leu26Pro
  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.48+4010T>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.77T>C
  hgvsp: ENSP00000404854.2:p.Leu26Pro
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.-61T>C
  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.77T>C
  hgvsp: ENSP00000429524.1:p.Leu26Pro
  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.77T>C
  hgvsp: ENSP00000319977.7:p.Leu26Pro
  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.77T>C
  hgvsp: ENSP00000347028.5:p.Leu26Pro
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.77T>C
  hgvsp: ENSP00000429172.1:p.Leu26Pro
  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.77T>C
  hgvsp: ENSP00000428384.1:p.Leu26Pro
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-122T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.-122T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.239T>C
  hgvsp: ENSP00000428991.1:p.Leu80Pro
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu26Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

8-134292501-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134292501
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134292501
    reference: chr 8
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.-99-15606G>C
  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.73G>C
  hgvsp: ENSP00000319977.7:p.Gly25Arg
  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.73G>C
  hgvsp: ENSP00000429524.1:p.Gly25Arg
  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.73G>C
  hgvsp: ENSP00000404854.2:p.Gly25Arg
  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.48+4006G>C
  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.124G>C
  hgvsp: ENSP00000428345.1:p.Gly42Arg
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-126G>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.106G>C
  hgvsp: ENSP00000429840.1:p.Gly36Arg
  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.73G>C
  hgvsp: ENSP00000429380.1:p.Gly25Arg
  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.73G>C
  hgvsp: ENSP00000429272.1:p.Gly25Arg
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.73G>C
  hgvsp: ENSP00000429172.1:p.Gly25Arg
  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.73G>C
  hgvsp: ENSP00000428384.1:p.Gly25Arg
  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.210G>C
  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.73G>C
  hgvsp: ENSP00000429994.1:p.Gly25Arg
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.-126G>C
  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.73G>C
  hgvsp: ENSP00000347028.5:p.Gly25Arg
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.235G>C
  hgvsp: ENSP00000428991.1:p.Gly79Arg
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.-65G>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.36+4018G>C
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gly25Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-134292501-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134292501
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134292501
    reference: chr 8
allele count: 2
allele frequency: 1.648043772042586e-5
allele num: 121356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.73G>A
  hgvsp: ENSP00000428384.1:p.Gly25Ser
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.73G>A
  hgvsp: ENSP00000429172.1:p.Gly25Ser
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-126G>A
  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.73G>A
  hgvsp: ENSP00000404854.2:p.Gly25Ser
  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.210G>A
  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.73G>A
  hgvsp: ENSP00000429524.1:p.Gly25Ser
  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.73G>A
  hgvsp: ENSP00000429272.1:p.Gly25Ser
  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.73G>A
  hgvsp: ENSP00000319977.7:p.Gly25Ser
  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.106G>A
  hgvsp: ENSP00000429840.1:p.Gly36Ser
  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.73G>A
  hgvsp: ENSP00000347028.5:p.Gly25Ser
  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.-99-15606G>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.48+4006G>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.73G>A
  hgvsp: ENSP00000429380.1:p.Gly25Ser
  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.73G>A
  hgvsp: ENSP00000429994.1:p.Gly25Ser
  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.124G>A
  hgvsp: ENSP00000428345.1:p.Gly42Ser
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.-65G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.-126G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.235G>A
  hgvsp: ENSP00000428991.1:p.Gly79Ser
  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.36+4018G>A
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gly25Ser
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

8-134292502-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134292502
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134292502
    reference: chr 8
allele count: 13
allele frequency: 1.071246106432421e-4
allele num: 121354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.72C>T
  hgvsp: ENST00000522890.1:c.72C>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.48+4005C>T
  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.72C>T
  hgvsp: ENST00000521544.1:c.72C>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.72C>T
  hgvsp: ENST00000354944.5:c.72C>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: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.72C>T
  hgvsp: ENST00000517599.1:c.72C>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.36+4017C>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.105C>T
  hgvsp: ENST00000520943.1:c.105C>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.72C>T
  hgvsp: ENST00000522377.1:c.72C>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.72C>T
  hgvsp: ENST00000519580.1:c.72C>T(p.%3D)
  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.-99-15607C>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: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.209C>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.123C>T
  hgvsp: ENST00000520230.1:c.123C>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.72C>T
  hgvsp: ENST00000323851.7:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.-127C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-127C>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.72C>T
  hgvsp: ENST00000519228.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.-66C>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.72C>T
  hgvsp: ENST00000414097.2:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.234C>T
  hgvsp: ENST00000522738.1:c.234C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Thr24Thr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

8-134292505-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134292505
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134292505
    reference: chr 8
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.231C>A
  hgvsp: ENST00000522738.1:c.231C>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.69C>A
  hgvsp: ENST00000414097.2:c.69C>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.36+4014C>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.69C>A
  hgvsp: ENST00000323851.7:c.69C>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.69C>A
  hgvsp: ENST00000519580.1:c.69C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.-130C>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.69C>A
  hgvsp: ENST00000354944.5:c.69C>A(p.%3D)
  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.-99-15610C>A
  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.69C>A
  hgvsp: ENST00000522377.1:c.69C>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.69C>A
  hgvsp: ENST00000519228.1:c.69C>A(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.102C>A
  hgvsp: ENST00000520943.1:c.102C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.-69C>A
  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.69C>A
  hgvsp: ENST00000522890.1:c.69C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-130C>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.120C>A
  hgvsp: ENST00000520230.1:c.120C>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.48+4002C>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.69C>A
  hgvsp: ENST00000521544.1:c.69C>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: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.69C>A
  hgvsp: ENST00000517599.1:c.69C>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.206C>A
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ile23Ile
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

8-134292508-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134292508
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134292508
    reference: chr 8
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429840
  ensembl transcript: ENST00000520943
  gene symbol: NDRG1
  hgvsc: ENST00000520943.1:c.99C>G
  hgvsp: ENST00000520943.1:c.99C>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.36+4011C>G
  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.203C>G
  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.66C>G
  hgvsp: ENST00000323851.7:c.66C>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: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.228C>G
  hgvsp: ENST00000522738.1:c.228C>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.66C>G
  hgvsp: ENST00000519580.1:c.66C>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.66C>G
  hgvsp: ENST00000519228.1:c.66C>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: ENSP00000429524
  ensembl transcript: ENST00000521544
  gene symbol: NDRG1
  hgvsc: ENST00000521544.1:c.66C>G
  hgvsp: ENST00000521544.1:c.66C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-133C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.-133C>G
  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.117C>G
  hgvsp: ENST00000520230.1:c.117C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.-72C>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: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.66C>G
  hgvsp: ENST00000517599.1:c.66C>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.66C>G
  hgvsp: ENST00000522890.1:c.66C>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.48+3999C>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.66C>G
  hgvsp: ENST00000522377.1:c.66C>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: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.66C>G
  hgvsp: ENST00000354944.5:c.66C>G(p.%3D)
  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.-99-15613C>G
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.66C>G
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff

8-134292510-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134292510
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134292510
    reference: chr 8
allele count: 9
allele frequency: 7.416441426593711e-5
allele num: 121352
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429840
  ensembl transcript: ENST00000520943
  gene symbol: NDRG1
  hgvsc: ENST00000520943.1:c.97A>G
  hgvsp: ENSP00000429840.1:p.Thr33Ala
  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.64A>G
  hgvsp: ENSP00000429272.1:p.Thr22Ala
  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.36+4009A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429524
  ensembl transcript: ENST00000521544
  gene symbol: NDRG1
  hgvsc: ENST00000521544.1:c.64A>G
  hgvsp: ENSP00000429524.1:p.Thr22Ala
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.226A>G
  hgvsp: ENSP00000428991.1:p.Thr76Ala
  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.64A>G
  hgvsp: ENSP00000404854.2:p.Thr22Ala
  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.-99-15615A>G
  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.115A>G
  hgvsp: ENSP00000428345.1:p.Thr39Ala
  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: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.64A>G
  hgvsp: ENSP00000429172.1:p.Thr22Ala
  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.64A>G
  hgvsp: ENSP00000319977.7:p.Thr22Ala
  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.64A>G
  hgvsp: ENSP00000429380.1:p.Thr22Ala
  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.201A>G
  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.64A>G
  hgvsp: ENSP00000429994.1:p.Thr22Ala
  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.64A>G
  hgvsp: ENSP00000347028.5:p.Thr22Ala
  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.64A>G
  hgvsp: ENSP00000428384.1:p.Thr22Ala
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.-74A>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.48+3997A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-135A>G
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Thr22Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
population: African
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

8-134292512-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134292512
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134292512
    reference: chr 8
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
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.48+3995A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-135-2A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429840
  ensembl transcript: ENST00000520943
  gene symbol: NDRG1
  hgvsc: ENST00000520943.1:c.97-2A>G
  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.64-2A>G
  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.-74-2A>G
  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.201-2A>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.-99-15617A>G
  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.64-2A>G
  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.64-2A>G
  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.115-2A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.64-2A>G
  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.64-2A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429524
  ensembl transcript: ENST00000521544
  gene symbol: NDRG1
  hgvsc: ENST00000521544.1:c.64-2A>G
  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.-135-2A>G
  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.64-2A>G
  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.64-2A>G
  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.64-2A>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.226-2A>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.36+4007A>G
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.64-2A>G
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

8-134292516-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134292516
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134292516
    reference: chr 8
allele count: 68312
allele frequency: 5.634908850944486e-1
allele num: 121230
alternate allele: G
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.64-6T>C
  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.201-6T>C
  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.64-6T>C
  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.64-6T>C
  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.64-6T>C
  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.97-6T>C
  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.64-6T>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.-99-15621T>C
  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.115-6T>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.36+4003T>C
  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.64-6T>C
  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.64-6T>C
  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.-135-6T>C
  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.64-6T>C
  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.64-6T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.226-6T>C
  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.-74-6T>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.48+3991T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-135-6T>C
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.64-6T>C
num of homozygotes: 20102
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

8-134292521-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134292521
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134292521
    reference: chr 8
allele count: 1
allele frequency: 8.249191579225235e-6
allele num: 121224
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.36+3998T>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.115-11T>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.97-11T>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.64-11T>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.64-11T>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.64-11T>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.64-11T>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.-74-11T>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.-99-15626T>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.64-11T>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.-135-11T>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.64-11T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-135-11T>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.64-11T>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.64-11T>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.64-11T>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.201-11T>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.48+3986T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.226-11T>C
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6602
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/8-134292522-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134292522
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134292522
    reference: chr 8
allele count: 1
allele frequency: 8.296276631047985e-6
allele num: 120536
alternate allele: A
canonical: false
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3783
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13043
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6206
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6458
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18088
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8157
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14899
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3292
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1550
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2227
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3560
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19288
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4596
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8580
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 1
  allele frequency: 1.50961625554784e-5
  allele num: 66242
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 11494
  num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 900
  num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/8-134292522-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134292522
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134292523
    reference: chr 8
allele count: 45
allele frequency: 3.733324483971593e-4
allele num: 120536
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428384
  ensembl transcript: ENST00000522890
  gene symbol: NDRG1
  hgvsc: ENST00000522890.1:c.64-13dupT
  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.201-13dupT
  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.64-13dupT
  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.-99-15628dupT
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.226-13dupT
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-135-13dupT
  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.64-13dupT
  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.48+3984dupT
  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.-74-13dupT
  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.64-13dupT
  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.97-13dupT
  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.64-13dupT
  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.-135-13dupT
  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.64-13dupT
  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.64-13dupT
  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.115-13dupT
  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.64-13dupT
  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.36+3996dupT
  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.64-13dupT
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 1
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/8-134292522-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134292522
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134292521
    reference: chr 8
allele count: 17
allele frequency: 1.410367027278158e-4
allele num: 120536
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.64-13delT
  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.64-13delT
  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.-99-15628delT
  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.64-13delT
  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.64-13delT
  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.64-13delT
  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.64-13delT
  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.97-13delT
  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.64-13delT
  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.48+3984delT
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.226-13delT
  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.115-13delT
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-135-13delT
  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.64-13delT
  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.36+3996delT
  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.-74-13delT
  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.201-13delT
  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.64-13delT
  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.-135-13delT
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3783
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: CA
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD

http://identifiers.org/exac.variant/8-134292527-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134292527
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134292527
    reference: chr 8
allele count: 1
allele frequency: 8.253957772752034e-6
allele num: 121154
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.64-17T>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.64-17T>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.-74-17T>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.64-17T>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.-99-15632T>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.64-17T>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.64-17T>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.64-17T>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.226-17T>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-135-17T>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.201-17T>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.-135-17T>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.115-17T>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.64-17T>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.64-17T>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.64-17T>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.48+3980T>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.36+3992T>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.97-17T>G
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2012
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP

8-134292530-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134292530
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134292530
    reference: chr 8
allele count: 1
allele frequency: 8.255320554097116e-6
allele num: 121134
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429840
  ensembl transcript: ENST00000520943
  gene symbol: NDRG1
  hgvsc: ENST00000520943.1:c.97-20T>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.64-20T>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.-135-20T>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.64-20T>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.36+3989T>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.48+3977T>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.64-20T>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.64-20T>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.226-20T>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.64-20T>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.115-20T>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.64-20T>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.64-20T>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-135-20T>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.-99-15635T>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.64-20T>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.-74-20T>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.64-20T>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.201-20T>A
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: QD

8-134292531-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134292531
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134292531
    reference: chr 8
allele count: 3
allele frequency: 2.476882430647292e-5
allele num: 121120
alternate allele: A
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.64-21A>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.97-21A>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.115-21A>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.64-21A>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.226-21A>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.64-21A>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.-74-21A>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.-135-21A>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.64-21A>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.64-21A>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.36+3988A>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.64-21A>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.201-21A>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.64-21A>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.48+3976A>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.64-21A>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-135-21A>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.64-21A>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.-99-15636A>T
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3312
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

8-134292537-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134292537
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134292537
    reference: chr 8
allele count: 3
allele frequency: 2.477496077297878e-5
allele num: 121090
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428345
  ensembl transcript: ENST00000520230
  gene symbol: NDRG1
  hgvsc: ENST00000520230.1:c.115-27T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.226-27T>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.64-27T>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.-135-27T>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.36+3982T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-135-27T>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.64-27T>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.-99-15642T>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.64-27T>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.64-27T>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.64-27T>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.64-27T>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.64-27T>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.201-27T>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.-74-27T>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.97-27T>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.64-27T>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.64-27T>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.48+3970T>C
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5878
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD

8-134292542-ATC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134292542
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134292540
    reference: chr 8
allele count: 3
allele frequency: 2.47827379968939e-5
allele num: 121052
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.64-34_64-33delGA
  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.-135-34_-135-33delGA
  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.64-34_64-33delGA
  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.64-34_64-33delGA
  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.97-34_97-33delGA
  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.64-34_64-33delGA
  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.64-34_64-33delGA
  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.64-34_64-33delGA
  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.201-34_201-33delGA
  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.115-34_115-33delGA
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.226-34_226-33delGA
  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.36+3975_36+3976delGA
  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.64-34_64-33delGA
  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.64-34_64-33delGA
  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.48+3963_48+3964delGA
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-135-34_-135-33delGA
  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.-74-34_-74-33delGA
  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.-99-15649_-99-15648delGA
  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.64-34_64-33delGA
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
reference allele: ATC
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

8-134292546-G-GT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134292546
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134292547
    reference: chr 8
allele count: 5
allele frequency: 4.132641253678051e-5
allele num: 120988
alternate allele: GT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.-99-15652dupA
  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.64-37dupA
  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.48+3960dupA
  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.115-37dupA
  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.97-37dupA
  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.64-37dupA
  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.36+3972dupA
  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.64-37dupA
  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.64-37dupA
  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.64-37dupA
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.226-37dupA
  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.64-37dupA
  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.-74-37dupA
  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.-135-37dupA
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-135-37dupA
  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.201-37dupA
  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.64-37dupA
  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.64-37dupA
  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.64-37dupA
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1464
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16310
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

8-134292559-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134292559
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134292559
    reference: chr 8
allele count: 6
allele frequency: 4.969931911932806e-5
allele num: 120726
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.97-49C>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.-135-49C>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.64-49C>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.64-49C>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.64-49C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-135-49C>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.64-49C>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.48+3948C>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.64-49C>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.201-49C>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.-74-49C>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.64-49C>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.115-49C>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.-99-15664C>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.64-49C>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.36+3960C>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.64-49C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.226-49C>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.64-49C>T
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10738
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3242
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum

8-134292559-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134292559
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134292559
    reference: chr 8
allele count: 1
allele frequency: 8.283219853221344e-6
allele num: 120726
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.64-49C>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.64-49C>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.-135-49C>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.64-49C>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.201-49C>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.48+3948C>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.115-49C>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.-99-15664C>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.64-49C>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.36+3960C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.226-49C>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.64-49C>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-135-49C>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.64-49C>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.97-49C>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.-74-49C>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.64-49C>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.64-49C>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.64-49C>G
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10738
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

8-134292562-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134292562
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134292562
    reference: chr 8
allele count: 51
allele frequency: 4.226052369903878e-4
allele num: 120680
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000427894
  ensembl transcript: ENST00000522476
  gene symbol: NDRG1
  hgvsc: ENST00000522476.1:c.-99-15667T>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.64-52T>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.36+3957T>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.-74-52T>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.64-52T>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.64-52T>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.97-52T>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.64-52T>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.64-52T>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.64-52T>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.115-52T>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.-135-52T>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.64-52T>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.48+3945T>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.201-52T>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.64-52T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.226-52T>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.64-52T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-135-52T>C
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/8-134296451-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134296451
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134296451
    reference: chr 8
allele count: 1
allele frequency: 8.262823902696986e-6
allele num: 121024
alternate allele: A
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.63+41G>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.36+68G>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.63+41G>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.-100+12926G>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.-75+41G>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.63+41G>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.63+41G>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.114+41G>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.63+41G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.225+41G>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.63+41G>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.63+41G>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.63+41G>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.96+41G>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.48+56G>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.-135-3941G>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.63+41G>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.200+41G>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-231+41G>T
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9560
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5846
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12086
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD

8-134296476-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134296476
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134296476
    reference: chr 8
allele count: 1
allele frequency: 8.247286642694553e-6
allele num: 121252
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.-135-3966C>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.63+16C>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.96+16C>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.63+16C>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.63+16C>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.63+16C>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.63+16C>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.114+16C>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.63+16C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.225+16C>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.36+43C>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.200+16C>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.-100+12901C>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.63+16C>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.63+16C>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.-75+16C>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.63+16C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-231+16C>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.48+31C>T
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum

8-134296486-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134296486
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134296486
    reference: chr 8
allele count: 30
allele frequency: 2.473288484368817e-4
allele num: 121296
alternate allele: G
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.63+6T>C
  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.63+6T>C
  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.96+6T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.225+6T>C
  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.63+6T>C
  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.63+6T>C
  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.63+6T>C
  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.114+6T>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.48+21T>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.-135-3976T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-231+6T>C
  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.63+6T>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.-100+12891T>C
  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.-75+6T>C
  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.63+6T>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.36+33T>C
  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.63+6T>C
  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.63+6T>C
  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.200+6T>C
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.63+6T>C
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

8-134296496-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134296496
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134296496
    reference: chr 8
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
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.36+23G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.221G>A
  hgvsp: ENSP00000428991.1:p.Gly74Glu
  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.59G>A
  hgvsp: ENSP00000347028.5:p.Gly20Glu
  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.92G>A
  hgvsp: ENSP00000429840.1:p.Gly31Glu
  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.48+11G>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.-100+12881G>A
  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.59G>A
  hgvsp: ENSP00000404854.2:p.Gly20Glu
  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.59G>A
  hgvsp: ENSP00000429994.1:p.Gly20Glu
  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.110G>A
  hgvsp: ENSP00000428345.1:p.Gly37Glu
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.-79G>A
  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.59G>A
  hgvsp: ENSP00000429272.1:p.Gly20Glu
  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.59G>A
  hgvsp: ENSP00000428384.1:p.Gly20Glu
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-235G>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.196G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.59G>A
  hgvsp: ENSP00000429172.1:p.Gly20Glu
  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.59G>A
  hgvsp: ENSP00000319977.7:p.Gly20Glu
  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.-135-3986G>A
  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.59G>A
  hgvsp: ENSP00000429524.1:p.Gly20Glu
  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.59G>A
  hgvsp: ENSP00000429380.1:p.Gly20Glu
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gly20Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

8-134296503-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134296503
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134296503
    reference: chr 8
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.214G>A
  hgvsp: ENSP00000428991.1:p.Glu72Lys
  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.52G>A
  hgvsp: ENSP00000347028.5:p.Glu18Lys
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.-86G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.52G>A
  hgvsp: ENSP00000429172.1:p.Glu18Lys
  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.52G>A
  hgvsp: ENSP00000429380.1:p.Glu18Lys
  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.52G>A
  hgvsp: ENSP00000319977.7:p.Glu18Lys
  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.85G>A
  hgvsp: ENSP00000429840.1:p.Glu29Lys
  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.52G>A
  hgvsp: ENSP00000429524.1:p.Glu18Lys
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-242G>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.52G>A
  hgvsp: ENSP00000428384.1:p.Glu18Lys
  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.36+16G>A
  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.52G>A
  hgvsp: ENSP00000429272.1:p.Glu18Lys
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.48+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.103G>A
  hgvsp: ENSP00000428345.1:p.Glu35Lys
  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.52G>A
  hgvsp: ENSP00000404854.2:p.Glu18Lys
  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.-135-3993G>A
  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.52G>A
  hgvsp: ENSP00000429994.1:p.Glu18Lys
  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.-100+12874G>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.189G>A
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Glu18Lys
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

8-134296506-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134296506
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134296506
    reference: chr 8
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000347028
  ensembl transcript: ENST00000354944
  gene symbol: NDRG1
  hgvsc: ENST00000354944.5:c.49G>A
  hgvsp: ENSP00000347028.5:p.Val17Met
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.48+1G>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.186G>A
  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.82G>A
  hgvsp: ENSP00000429840.1:p.Val28Met
  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.-100+12871G>A
  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.49G>A
  hgvsp: ENSP00000404854.2:p.Val17Met
  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.49G>A
  hgvsp: ENSP00000319977.7:p.Val17Met
  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.49G>A
  hgvsp: ENSP00000429272.1:p.Val17Met
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.-89G>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.100G>A
  hgvsp: ENSP00000428345.1:p.Val34Met
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.49G>A
  hgvsp: ENSP00000429172.1:p.Val17Met
  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.49G>A
  hgvsp: ENSP00000429994.1:p.Val17Met
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.211G>A
  hgvsp: ENSP00000428991.1:p.Val71Met
  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.36+13G>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.49G>A
  hgvsp: ENSP00000428384.1:p.Val17Met
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-245G>A
  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.49G>A
  hgvsp: ENSP00000429524.1:p.Val17Met
  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.49G>A
  hgvsp: ENSP00000429380.1:p.Val17Met
  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.-135-3996G>A
  variant of: http://identifiers.org/hgnc/7679
canonical: false
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.48+1G>A
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

8-134296507-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134296507
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134296507
    reference: chr 8
allele count: 2
allele frequency: 1.648016612007449e-5
allele num: 121358
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-246G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.48G>A
  hgvsp: ENST00000517599.1:c.48G>A(p.%3D)
  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.-100+12870G>A
  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.48G>A
  hgvsp: ENST00000522377.1:c.48G>A(p.%3D)
  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.-135-3997G>A
  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.48G>A
  hgvsp: ENST00000519580.1:c.48G>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.48G>A
  hgvsp: ENST00000519228.1:c.48G>A(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: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.48G>A
  hgvsp: ENST00000518176.1:c.48G>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.99G>A
  hgvsp: ENST00000520230.1:c.99G>A(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.81G>A
  hgvsp: ENST00000520943.1:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.-90G>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.48G>A
  hgvsp: ENST00000521544.1:c.48G>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.48G>A
  hgvsp: ENST00000354944.5:c.48G>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.48G>A
  hgvsp: ENST00000522890.1:c.48G>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.36+12G>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.185G>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.48G>A
  hgvsp: ENST00000414097.2:c.48G>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.48G>A
  hgvsp: ENST00000323851.7:c.48G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.210G>A
  hgvsp: ENST00000522738.1:c.210G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.48G>A
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD

8-134296513-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134296513
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134296513
    reference: chr 8
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.42G>A
  hgvsp: ENST00000518176.1:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-252G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.36+6G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.-96G>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.93G>A
  hgvsp: ENST00000520230.1:c.93G>A(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.75G>A
  hgvsp: ENST00000520943.1:c.75G>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.42G>A
  hgvsp: ENST00000522377.1:c.42G>A(p.%3D)
  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.-135-4003G>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.42G>A
  hgvsp: ENST00000414097.2:c.42G>A(p.%3D)
  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.42G>A
  hgvsp: ENST00000521544.1:c.42G>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.42G>A
  hgvsp: ENST00000354944.5:c.42G>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.42G>A
  hgvsp: ENST00000522890.1:c.42G>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: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.42G>A
  hgvsp: ENST00000517599.1:c.42G>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.42G>A
  hgvsp: ENST00000519228.1:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.204G>A
  hgvsp: ENST00000522738.1:c.204G>A(p.%3D)
  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.-100+12864G>A
  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.42G>A
  hgvsp: ENST00000519580.1:c.42G>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.42G>A
  hgvsp: ENST00000323851.7:c.42G>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.179G>A
  variant of: http://identifiers.org/hgnc/7679
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.36+6G>A
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff

8-134296517-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134296517
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134296517
    reference: chr 8
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428802
  ensembl transcript: ENST00000518480
  gene symbol: NDRG1
  hgvsc: ENST00000518480.1:c.-135-4007T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.38T>C
  hgvsp: ENSP00000429007.1:p.Val13Ala
  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.38T>C
  hgvsp: ENSP00000429524.1:p.Val13Ala
  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.71T>C
  hgvsp: ENSP00000429840.1:p.Val24Ala
  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.38T>C
  hgvsp: ENSP00000319977.7:p.Val13Ala
  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.38T>C
  hgvsp: ENSP00000429380.1:p.Val13Ala
  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.38T>C
  hgvsp: ENSP00000404854.2:p.Val13Ala
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.38T>C
  hgvsp: ENSP00000429172.1:p.Val13Ala
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.36+2T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.-100T>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.-100+12860T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.200T>C
  hgvsp: ENSP00000428991.1:p.Val67Ala
  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.89T>C
  hgvsp: ENSP00000428345.1:p.Val30Ala
  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.38T>C
  hgvsp: ENSP00000429994.1:p.Val13Ala
  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.38T>C
  hgvsp: ENSP00000429272.1:p.Val13Ala
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-256T>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: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.175T>C
  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.38T>C
  hgvsp: ENSP00000347028.5:p.Val13Ala
  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.38T>C
  hgvsp: ENSP00000428384.1:p.Val13Ala
  variant of: http://identifiers.org/hgnc/7679
canonical: false
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.36+2T>C
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum

8-134296523-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134296523
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134296523
    reference: chr 8
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429994
  ensembl transcript: ENST00000519228
  gene symbol: NDRG1
  hgvsc: ENST00000519228.1:c.32C>T
  hgvsp: ENSP00000429994.1:p.Ala11Val
  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.32C>T
  hgvsp: ENSP00000404854.2:p.Ala11Val
  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.32C>T
  hgvsp: ENSP00000319977.7:p.Ala11Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.32C>T
  hgvsp: ENSP00000429172.1:p.Ala11Val
  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.32C>T
  hgvsp: ENSP00000429524.1:p.Ala11Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.-106C>T
  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.65C>T
  hgvsp: ENSP00000429840.1:p.Ala22Val
  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.32C>T
  hgvsp: ENSP00000428384.1:p.Ala11Val
  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.-100+12854C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.32C>T
  hgvsp: ENSP00000429007.1:p.Ala11Val
  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.32C>T
  hgvsp: ENSP00000429380.1:p.Ala11Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.32C>T
  hgvsp: ENSP00000431057.1:p.Ala11Val
  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.32C>T
  hgvsp: ENSP00000429272.1:p.Ala11Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.194C>T
  hgvsp: ENSP00000428991.1:p.Ala65Val
  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.83C>T
  hgvsp: ENSP00000428345.1:p.Ala28Val
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-262C>T
  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.32C>T
  hgvsp: ENSP00000347028.5:p.Ala11Val
  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.-135-4013C>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: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.169C>T
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala11Val
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

8-134296524-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134296524
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134296524
    reference: chr 8
allele count: 124
allele frequency: 1.021652440431071e-3
allele num: 121372
alternate allele: T
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.31G>A
  hgvsp: ENSP00000429380.1:p.Ala11Thr
  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.168G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.31G>A
  hgvsp: ENSP00000431057.1:p.Ala11Thr
  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.64G>A
  hgvsp: ENSP00000429840.1:p.Ala22Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.-107G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.31G>A
  hgvsp: ENSP00000429007.1:p.Ala11Thr
  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.82G>A
  hgvsp: ENSP00000428345.1:p.Ala28Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.193G>A
  hgvsp: ENSP00000428991.1:p.Ala65Thr
  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.31G>A
  hgvsp: ENSP00000429524.1:p.Ala11Thr
  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.-135-4014G>A
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-263G>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.31G>A
  hgvsp: ENSP00000347028.5:p.Ala11Thr
  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.31G>A
  hgvsp: ENSP00000319977.7:p.Ala11Thr
  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.31G>A
  hgvsp: ENSP00000429994.1:p.Ala11Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.31G>A
  hgvsp: ENSP00000429172.1:p.Ala11Thr
  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.31G>A
  hgvsp: ENSP00000429272.1:p.Ala11Thr
  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.31G>A
  hgvsp: ENSP00000404854.2:p.Ala11Thr
  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.31G>A
  hgvsp: ENSP00000428384.1:p.Ala11Thr
  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.-100+12853G>A
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala11Thr
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

8-134296525-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134296525
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134296525
    reference: chr 8
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000404854
  ensembl transcript: ENST00000414097
  gene symbol: NDRG1
  hgvsc: ENST00000414097.2:c.30C>T
  hgvsp: ENST00000414097.2:c.30C>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.30C>T
  hgvsp: ENST00000323851.7:c.30C>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.81C>T
  hgvsp: ENST00000520230.1:c.81C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-264C>T
  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.30C>T
  hgvsp: ENST00000522377.1:c.30C>T(p.%3D)
  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.-100+12852C>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: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.167C>T
  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.30C>T
  hgvsp: ENST00000521544.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.30C>T
  hgvsp: ENST00000518176.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.30C>T
  hgvsp: ENST00000518066.1:c.30C>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.30C>T
  hgvsp: ENST00000519228.1:c.30C>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: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.30C>T
  hgvsp: ENST00000517599.1:c.30C>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.30C>T
  hgvsp: ENST00000354944.5:c.30C>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.30C>T
  hgvsp: ENST00000519580.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.192C>T
  hgvsp: ENST00000522738.1:c.192C>T(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.63C>T
  hgvsp: ENST00000520943.1:c.63C>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.30C>T
  hgvsp: ENST00000522890.1:c.30C>T(p.%3D)
  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.-135-4015C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.-108C>T
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu10Leu
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

8-134296541-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134296541
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134296541
    reference: chr 8
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: G
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.151T>C
  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.14T>C
  hgvsp: ENSP00000428384.1:p.Met5Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.14T>C
  hgvsp: ENSP00000431057.1:p.Met5Thr
  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.65T>C
  hgvsp: ENSP00000428345.1:p.Met22Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.14T>C
  hgvsp: ENSP00000429007.1:p.Met5Thr
  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.14T>C
  hgvsp: ENSP00000429380.1:p.Met5Thr
  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.14T>C
  hgvsp: ENSP00000429272.1:p.Met5Thr
  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.-135-4031T>C
  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.14T>C
  hgvsp: ENSP00000319977.7:p.Met5Thr
  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.47T>C
  hgvsp: ENSP00000429840.1:p.Met16Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.176T>C
  hgvsp: ENSP00000428991.1:p.Met59Thr
  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.14T>C
  hgvsp: ENSP00000347028.5:p.Met5Thr
  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.14T>C
  hgvsp: ENSP00000404854.2:p.Met5Thr
  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.14T>C
  hgvsp: ENSP00000429994.1:p.Met5Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-280T>C
  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.14T>C
  hgvsp: ENSP00000429524.1:p.Met5Thr
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.-124T>C
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.14T>C
  hgvsp: ENSP00000429172.1:p.Met5Thr
  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.-100+12836T>C
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Met5Thr
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

8-134296547-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134296547
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134296547
    reference: chr 8
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.170G>A
  hgvsp: ENSP00000428991.1:p.Arg57Gln
  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.59G>A
  hgvsp: ENSP00000428345.1:p.Arg20Gln
  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.8G>A
  hgvsp: ENSP00000429380.1:p.Arg3Gln
  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.145G>A
  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.8G>A
  hgvsp: ENSP00000429524.1:p.Arg3Gln
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.8G>A
  hgvsp: ENSP00000429172.1:p.Arg3Gln
  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.8G>A
  hgvsp: ENSP00000404854.2:p.Arg3Gln
  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.-100+12830G>A
  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.41G>A
  hgvsp: ENSP00000429840.1:p.Arg14Gln
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.8G>A
  hgvsp: ENSP00000429007.1:p.Arg3Gln
  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.-135-4037G>A
  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.8G>A
  hgvsp: ENSP00000429994.1:p.Arg3Gln
  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.8G>A
  hgvsp: ENSP00000347028.5:p.Arg3Gln
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.-130G>A
  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.8G>A
  hgvsp: ENSP00000429272.1:p.Arg3Gln
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.8G>A
  hgvsp: ENSP00000431057.1:p.Arg3Gln
  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.8G>A
  hgvsp: ENSP00000319977.7:p.Arg3Gln
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-286G>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.8G>A
  hgvsp: ENSP00000428384.1:p.Arg3Gln
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg3Gln
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: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS

8-134296548-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134296548
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134296548
    reference: chr 8
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000319977
  ensembl transcript: ENST00000323851
  gene symbol: NDRG1
  hgvsc: ENST00000323851.7:c.7C>T
  hgvsp: ENSP00000319977.7:p.Arg3Trp
  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.-100+12829C>T
  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.7C>T
  hgvsp: ENSP00000429380.1:p.Arg3Trp
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.7C>T
  hgvsp: ENSP00000431057.1:p.Arg3Trp
  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.7C>T
  hgvsp: ENSP00000429994.1:p.Arg3Trp
  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.40C>T
  hgvsp: ENSP00000429840.1:p.Arg14Trp
  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.-135-4038C>T
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.7C>T
  hgvsp: ENSP00000429172.1:p.Arg3Trp
  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.7C>T
  hgvsp: ENSP00000428384.1:p.Arg3Trp
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.7C>T
  hgvsp: ENSP00000429007.1:p.Arg3Trp
  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.7C>T
  hgvsp: ENSP00000429272.1:p.Arg3Trp
  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.58C>T
  hgvsp: ENSP00000428345.1:p.Arg20Trp
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.169C>T
  hgvsp: ENSP00000428991.1:p.Arg57Trp
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.-131C>T
  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.7C>T
  hgvsp: ENSP00000347028.5:p.Arg3Trp
  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.7C>T
  hgvsp: ENSP00000429524.1:p.Arg3Trp
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-287C>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: ENST00000518010
  gene symbol: NDRG1
  hgvsc: ENST00000518010.1:n.144C>T
  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.7C>T
  hgvsp: ENSP00000404854.2:p.Arg3Trp
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg3Trp
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

http://identifiers.org/exac.variant/8-134296551-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134296551
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134296551
    reference: chr 8
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429272
  ensembl transcript: ENST00000519580
  gene symbol: NDRG1
  hgvsc: ENST00000519580.1:c.4T>G
  hgvsp: ENSP00000429272.1:p.Ser2Ala
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000430171
  ensembl transcript: ENST00000523892
  gene symbol: NDRG1
  hgvsc: ENST00000523892.1:c.-290T>G
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429007
  ensembl transcript: ENST00000518176
  gene symbol: NDRG1
  hgvsc: ENST00000518176.1:c.4T>G
  hgvsp: ENSP00000429007.1:p.Ser2Ala
  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.4T>G
  hgvsp: ENSP00000429524.1:p.Ser2Ala
  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.55T>G
  hgvsp: ENSP00000428345.1:p.Ser19Ala
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000429172
  ensembl transcript: ENST00000517599
  gene symbol: NDRG1
  hgvsc: ENST00000517599.1:c.4T>G
  hgvsp: ENSP00000429172.1:p.Ser2Ala
  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.141T>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.-100+12826T>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.4T>G
  hgvsp: ENSP00000428384.1:p.Ser2Ala
  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.-135-4041T>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.37T>G
  hgvsp: ENSP00000429840.1:p.Ser13Ala
  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.4T>G
  hgvsp: ENSP00000429994.1:p.Ser2Ala
  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.4T>G
  hgvsp: ENSP00000429380.1:p.Ser2Ala
  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.4T>G
  hgvsp: ENSP00000404854.2:p.Ser2Ala
  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.4T>G
  hgvsp: ENSP00000319977.7:p.Ser2Ala
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000431057
  ensembl transcript: ENST00000518066
  gene symbol: NDRG1
  hgvsc: ENST00000518066.1:c.4T>G
  hgvsp: ENSP00000431057.1:p.Ser2Ala
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000428991
  ensembl transcript: ENST00000522738
  gene symbol: NDRG1
  hgvsc: ENST00000522738.1:c.166T>G
  hgvsp: ENSP00000428991.1:p.Ser56Ala
  variant of: http://identifiers.org/hgnc/7679
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104419
  ensembl protein: ENSP00000437443
  ensembl transcript: ENST00000537882
  gene symbol: NDRG1
  hgvsc: ENST00000537882.1:c.-134T>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.4T>G
  hgvsp: ENSP00000347028.5:p.Ser2Ala
  variant of: http://identifiers.org/hgnc/7679
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ser2Ala
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
reference allele: A
site quality: QD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/8-134296558-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134296558
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134296558
    reference: chr 8
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: A
canonical: false
consequence: missense
filter: PASS
hgvs: p.Arg53Ser
num of homozygotes: 0
reference allele: C

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

GenotypeDepth
all individuals: 10881
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6394
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 763
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1294
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 656
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12119
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 681
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 602
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 673
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3599
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2069
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2616
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14529
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 763
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 676
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1018
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 816
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1990
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 137
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 347
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4009
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4770
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18290
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2751
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3428
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16692
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7099
bin: 6.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.08e0

FS
type: SiteQuality
SIO_000300: 3.035e0

VQSLOD
type: SiteQuality
SIO_000300: 4.57e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.35e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.609e0

QD
type: SiteQuality
SIO_000300: 1.173e1

DP
type: SiteQuality
SIO_000300: 2.298689e6

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

GenotypeDepth
all individuals: 11954
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2070
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10866
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6385
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 816
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 681
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3599
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14473
bin: 2.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 572
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1018
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 951
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 763
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1293
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 656
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 676
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 673
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2616
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 350
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 349
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2750
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4756
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7085
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1988
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16691
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 3415
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4006
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18136
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 2.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66688
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.917e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.552e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.387e0

FS
type: SiteQuality
SIO_000300: 7.12e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 5.45e-1

DP
type: SiteQuality
SIO_000300: 2.296776e6

QD
type: SiteQuality
SIO_000300: 9.43e0

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

GenotypeDepth
all individuals: 1018
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11461
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2068
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1520
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6389
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14313
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10851
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2616
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 673
bin: 7.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1294
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 656
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 681
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3600
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 666
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 602
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 676
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 816
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17192
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4744
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 583
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6968
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 281
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 2748
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4002
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1988
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 561
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3396
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16694
bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66688
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.35e0

DP
type: SiteQuality
SIO_000300: 2.292384e6

FS
type: SiteQuality
SIO_000300: 7.14e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.57e-1

QD
type: SiteQuality
SIO_000300: 1.045e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.735e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.31e-1

GenotypeDepth
all individuals: 2616
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1294
bin: 5.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2068
bin: 4.75e1
variant carriers: 1

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

GenotypeDepth
all individuals: 3600
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14313
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11461
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 673
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 666
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 602
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6389
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1018
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 763
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 656
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 681
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10851
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 676
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 816
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17192
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4744
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4002
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3396
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 561
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 583
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6968
bin: 6.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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South Asian
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European (Finnish)
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Other
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African
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European (Non-Finnish)
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DP
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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MQRankSum
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QD
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FS
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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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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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East Asian
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European (Non-Finnish)
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European (Finnish)
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Latino
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DP
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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QD
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FS
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MQ
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MQRankSum
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ReadPosRankSum
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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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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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allele num: 11560
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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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African
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Other
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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MQ
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BaseQRankSum
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VQSLOD
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DP
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FS
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QD
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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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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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European (Non-Finnish)
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East Asian
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Other
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European (Finnish)
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African
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MQ
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ReadPosRankSum
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VQSLOD
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QD
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InbreedingCoeff
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DP
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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Latino
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European (Non-Finnish)
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East Asian
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European (Finnish)
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African
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South Asian
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VQSLOD
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MQRankSum
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BaseQRankSum
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FS
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DP
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QD
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InbreedingCoeff
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ReadPosRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 8.664009703690868e-5
allele num: 11542
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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MQRankSum
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VQSLOD
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BaseQRankSum
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MQ
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SIO_000300: 5.911e1

ClippingRankSum
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SIO_000300: 8.44e-1

InbreedingCoeff
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SIO_000300: 1.39e-2

ReadPosRankSum
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SIO_000300: -1.89e-1

FS
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DP
type: SiteQuality
SIO_000300: 2.279678e6

QD
type: SiteQuality
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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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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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

Other
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allele frequency: 1.108647450110865e-3
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African
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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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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.503081316699233e-5
allele num: 66530
num of homozygotes: 0

South Asian
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allele num: 16490
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
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SIO_000300: 1.02e-2

MQRankSum
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BaseQRankSum
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ClippingRankSum
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FS
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MQ
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VQSLOD
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ReadPosRankSum
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QD
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DP
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SIO_000300: 2.280532e6

GenotypeDepth
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variant carriers: 1

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

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

European (Non-Finnish)
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allele count: 5
allele frequency: 7.512019230769231e-5
allele num: 66560
num of homozygotes: 0

MQ
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SIO_000300: 5.927e1

MQRankSum
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BaseQRankSum
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SIO_000300: -2.268e0

InbreedingCoeff
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QD
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FS
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ClippingRankSum
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SIO_000300: -6.7e-1

VQSLOD
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DP
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SIO_000300: 2.281244e6

ReadPosRankSum
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SIO_000300: 4.54e-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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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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Latino
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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
allele num: 66016
num of homozygotes: 0

Other
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African
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allele count: 0
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East Asian
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allele count: 1
allele frequency: 1.177301624676242e-4
allele num: 8494
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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MQ
type: SiteQuality
SIO_000300: 5.881e1

MQRankSum
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InbreedingCoeff
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FS
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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DP
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QD
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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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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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

Latino
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num of homozygotes: 0

African
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South Asian
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allele frequency: 1.824151769427216e-4
allele num: 16446
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East Asian
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allele count: 0
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European (Non-Finnish)
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allele frequency: 3.024986387561256e-5
allele num: 66116
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European (Finnish)
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BaseQRankSum
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SIO_000300: -2.302e0

VQSLOD
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MQRankSum
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DP
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ClippingRankSum
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FS
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QD
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MQ
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InbreedingCoeff
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

East Asian
type: Population
allele count: 3
allele frequency: 3.515350363252871e-4
allele num: 8534
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.045949214026602e-5
allele num: 66160
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.722958827634333e-5
allele num: 11464
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.98e-1

QD
type: SiteQuality
SIO_000300: 1.258e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.47e0

DP
type: SiteQuality
SIO_000300: 2.23902e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.05e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
all individuals: 2678
bin: 4.25e1
variant carriers: 10

GenotypeDepth
all individuals: 1182
bin: 5.25e1
variant carriers: 6

GenotypeDepth
all individuals: 862
bin: 6.25e1
variant carriers: 3

GenotypeDepth
all individuals: 9690
bin: 3.25e1
variant carriers: 22

GenotypeDepth
all individuals: 811
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 774
bin: 7.25e1
variant carriers: 4

GenotypeDepth
all individuals: 805
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 865
bin: 6.75e1
variant carriers: 2

GenotypeDepth
all individuals: 747
bin: 8.25e1
variant carriers: 6

GenotypeDepth
all individuals: 13482
bin: 2.75e1
variant carriers: 18

GenotypeDepth
all individuals: 548
bin: 9.25e1
variant carriers: 6

GenotypeDepth
all individuals: 268
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1567
bin: 4.75e1
variant carriers: 13

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

GenotypeDepth
all individuals: 4875
bin: 3.75e1
variant carriers: 22

GenotypeDepth
all individuals: 683
bin: 8.75e1
variant carriers: 8

GenotypeDepth
all individuals: 16947
bin: 2.25e1
variant carriers: 10

GenotypeQuality
all individuals: 226
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 399
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4899
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16375
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3366
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2030
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17590
bin: 9.75e1
variant carriers: 173

GenotypeQuality
all individuals: 216
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4186
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7031
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2777
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 72
allele frequency: 4.370523248755614e-3
allele num: 16474
num of homozygotes: 1

Latino
type: Population
allele count: 5
allele frequency: 4.353883664228492e-4
allele num: 11484
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 88
allele frequency: 1.325740456175239e-3
allele num: 66378
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.513317191283293e-4
allele num: 6608
num of homozygotes: 0

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

African
type: Population
allele count: 4
allele frequency: 3.857280617164899e-4
allele num: 10370
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.333333333333334e-3
allele num: 900
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.329e1

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.5e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.39e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.598e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.73e-2

DP
type: SiteQuality
SIO_000300: 2.265874e6

GenotypeDepth
all individuals: 134
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2468
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1182
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10044
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2720
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1576
bin: 4.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 745
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 775
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4960
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13901
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 906
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 861
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 269
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 683
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 812
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 545
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 162
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 129
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7215
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2102
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 90
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4339
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17601
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 91
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17149
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5083
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3510
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2860
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 66
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502358703163967e-5
allele num: 66562
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.74e0

MQ
type: SiteQuality
SIO_000300: 5.948e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.687e0

MQRankSum
type: SiteQuality
SIO_000300: -6.08e-1

DP
type: SiteQuality
SIO_000300: 2.28351e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.7e-2

FS
type: SiteQuality
SIO_000300: 5.613e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.92e-1

GenotypeDepth
all individuals: 683
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1182
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 13976
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4967
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10101
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 745
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 865
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 186
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 906
bin: 5.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 775
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 861
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2726
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2468
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1578
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 120
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4376
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 55
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 3.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 66
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17219
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3538
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5120
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7262
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2117
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2874
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17618
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.622786759045419e-5
allele num: 10392
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.582e0

DP
type: SiteQuality
SIO_000300: 2.286185e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.25e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.196e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.47e-1

FS
type: SiteQuality
SIO_000300: 3.056e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 7.92e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.7e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000104419
ensembl protein: ENSP00000429007
ensembl transcript: ENST00000518176
gene symbol: NDRG1
hgvsc: ENST00000518176.1:c.48+4031A>G
variant of: http://identifiers.org/hgnc/7679

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

GenotypeDepth
all individuals: 16885
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 745
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 906
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10313
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5018
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 775
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2746
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 545
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14182
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 52
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1589
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2469
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 683
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 811
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 861
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 865
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1185
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17664
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 44
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2147
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2905
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17179
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5209
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7372
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3603
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4428
bin: 8.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66698
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.409e0

FS
type: SiteQuality
SIO_000300: 3.025e0

VQSLOD
type: SiteQuality
SIO_000300: 1.22e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.138e0

QD
type: SiteQuality
SIO_000300: 1.386e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.293789e6

GenotypeDepth
all individuals: 865
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1186
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 683
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5023
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10337
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 812
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1593
bin: 4.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 861
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 775
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 44
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 41
bin: 1.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 906
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 545
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2468
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 16829
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2748
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14207
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 745
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17159
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7383
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 17672
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 21
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5220
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 43
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2907
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3605
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2148
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4432
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66698
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
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FS
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VQSLOD
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InbreedingCoeff
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MQRankSum
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DP
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MQ
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Latino
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African
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InbreedingCoeff
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MQ
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VQSLOD
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FS
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GenotypeQuality
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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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European (Finnish)
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East Asian
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European (Non-Finnish)
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FS
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MQRankSum
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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DP
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MQ
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GenotypeQuality
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num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: -7.679e-1

QD
type: SiteQuality
SIO_000300: 1.137e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.324e0

FS
type: SiteQuality
SIO_000300: 1.65e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.4e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.33e0

MQRankSum
type: SiteQuality
SIO_000300: -1.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.952e1

DP
type: SiteQuality
SIO_000300: 2.296202e6

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

GenotypeDepth
all individuals: 14279
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1596
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 812
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 911
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 121
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1196
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2467
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 44
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2757
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5039
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 866
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 747
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16583
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 870
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 684
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 546
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 775
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10385
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 67
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 46
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3611
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5216
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7401
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2149
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16962
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2909
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4442
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17705
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49902563333833e-5
allele num: 66710
num of homozygotes: 0

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

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

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

FS
type: SiteQuality
SIO_000300: 6.532e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.44e-1

QD
type: SiteQuality
SIO_000300: 1.113e1

MQ
type: SiteQuality
SIO_000300: 5.924e1

VQSLOD
type: SiteQuality
SIO_000300: 1.06e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

DP
type: SiteQuality
SIO_000300: 2.296813e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.13e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.79e-1

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

GenotypeDepth
all individuals: 14279
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 44
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 812
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1196
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16583
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 121
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 866
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 870
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5039
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 546
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10385
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1596
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 747
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 684
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2467
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 911
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2757
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 775
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2909
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5216
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2149
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 3611
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7401
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4442
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16962
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17705
bin: 9.75e1
variant carriers: 2

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.99805126667666e-5
allele num: 66710
num of homozygotes: 0

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.924e1

MQRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.13e-1

FS
type: SiteQuality
SIO_000300: 6.532e0

DP
type: SiteQuality
SIO_000300: 2.296813e6

BaseQRankSum
type: SiteQuality
SIO_000300: -9.44e-1

QD
type: SiteQuality
SIO_000300: 1.113e1

VQSLOD
type: SiteQuality
SIO_000300: 1.06e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

GenotypeDepth
all individuals: 683
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 546
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 747
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16559
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 118
bin: 1.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 5043
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 871
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 7.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 1198
bin: 5.25e1
variant carriers: 2

GenotypeDepth
all individuals: 867
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2760
bin: 4.25e1
variant carriers: 3

GenotypeDepth
all individuals: 1596
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10390
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2470
bin: 9.75e1
variant carriers: 5

GenotypeDepth
all individuals: 915
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 14284
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 776
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 812
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 5217
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2910
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16962
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7387
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2149
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3605
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17725
bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 4440
bin: 8.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 9
allele frequency: 5.450581395348837e-4
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.49707690001499e-5
allele num: 66710
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.5e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.97e0

DP
type: SiteQuality
SIO_000300: 2.297793e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.936e1

MQRankSum
type: SiteQuality
SIO_000300: 5.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -5.8e-1

QD
type: SiteQuality
SIO_000300: 1.135e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.58e-1

GenotypeDepth
all individuals: 812
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14309
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16508
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10391
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1600
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 140
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 775
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1199
bin: 5.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 747
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2468
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5043
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 683
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2761
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 867
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 546
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 870
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 913
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 3.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 4442
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16827
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5220
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17723
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 2912
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7363
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2147
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3607
bin: 7.25e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49907057624273e-5
allele num: 66708
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -7.4e-2

FS
type: SiteQuality
SIO_000300: 5.33e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.57e0

DP
type: SiteQuality
SIO_000300: 2.297574e6

MQ
type: SiteQuality
SIO_000300: 5.946e1

MQRankSum
type: SiteQuality
SIO_000300: 2.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.237e0

QD
type: SiteQuality
SIO_000300: 1.05e1

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.66C>G
hgvsp: ENST00000414097.2:c.66C>G(p.%3D)
variant of: http://identifiers.org/hgnc/7679

GenotypeDepth
all individuals: 140
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 867
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 870
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 28
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 683
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1199
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 812
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 46
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2760
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1603
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16483
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 775
bin: 7.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 10405
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 747
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 913
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 546
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2468
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5046
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14314
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2146
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17725
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 3607
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 34
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7363
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4445
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5224
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2912
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16816
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 2.25e1
variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49902563333833e-5
allele num: 66710
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.228e1

DP
type: SiteQuality
SIO_000300: 2.297844e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.537e0

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

MQRankSum
type: SiteQuality
SIO_000300: -2.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.54e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

Annotation
canonical: false
consequence: splice_region_variant
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000104419
ensembl protein: ENSP00000428802
ensembl transcript: ENST00000518480
gene symbol: NDRG1
hgvsc: ENST00000518480.1:c.-135A>G
variant of: http://identifiers.org/hgnc/7679

GenotypeDepth
all individuals: 14322
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10396
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 546
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5051
bin: 3.75e1
variant carriers: 2

GenotypeDepth
all individuals: 812
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2762
bin: 4.25e1
variant carriers: 2

GenotypeDepth
all individuals: 49
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 138
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1201
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 747
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1603
bin: 4.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 774
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16468
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2469
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 872
bin: 6.75e1
variant carriers: 2

GenotypeDepth
all individuals: 867
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 917
bin: 5.75e1
variant carriers: 2

GenotypeDepth
all individuals: 683
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 28
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 61
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16765
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7368
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2147
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 103
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 35
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5229
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2912
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17736
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 4448
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3604
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.349123070004497e-4
allele num: 66710
num of homozygotes: 0

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

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

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.97e-1

FS
type: SiteQuality
SIO_000300: 5.3e-1

DP
type: SiteQuality
SIO_000300: 2.298228e6

MQRankSum
type: SiteQuality
SIO_000300: -2.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.99e-1

MQ
type: SiteQuality
SIO_000300: 5.936e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 6.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.79e-1

QD
type: SiteQuality
SIO_000300: 1.474e1

GenotypeDepth
all individuals: 2764
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 774
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16424
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10416
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 683
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1604
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 546
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 868
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 141
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2469
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 812
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 916
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 872
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5052
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 747
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14334
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16667
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3608
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5230
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4446
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7365
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2149
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 66
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2912
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17736
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 34
bin: 3.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.92e1

MQRankSum
type: SiteQuality
SIO_000300: 1.91e-1

FS
type: SiteQuality
SIO_000300: 1.024e0

DP
type: SiteQuality
SIO_000300: 2.298661e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e0

VQSLOD
type: SiteQuality
SIO_000300: 6.26e-1

QD
type: SiteQuality
SIO_000300: 1.251e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.35e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.53e-1

GenotypeDepth
all individuals: 5492
bin: 5.25e1
variant carriers: 5245

GenotypeDepth
all individuals: 5685
bin: 4.25e1
variant carriers: 5194

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

GenotypeDepth
all individuals: 4808
bin: 3.75e1
variant carriers: 3957

GenotypeDepth
all individuals: 3052
bin: 6.75e1
variant carriers: 2823

GenotypeDepth
all individuals: 928
bin: 8.75e1
variant carriers: 784

GenotypeDepth
all individuals: 4842
bin: 5.75e1
variant carriers: 4602

GenotypeDepth
all individuals: 3870
bin: 6.25e1
variant carriers: 3658

GenotypeDepth
all individuals: 5777
bin: 4.75e1
variant carriers: 5489

GenotypeDepth
all individuals: 1627
bin: 7.75e1
variant carriers: 1418

GenotypeDepth
all individuals: 1197
bin: 8.25e1
variant carriers: 1010

GenotypeDepth
all individuals: 3717
bin: 2.25e1
variant carriers: 489

GenotypeDepth
all individuals: 17
bin: 7.5e0
variant carriers: 4

GenotypeDepth
all individuals: 69
bin: 1.25e1
variant carriers: 30

GenotypeDepth
all individuals: 4466
bin: 3.25e1
variant carriers: 2450

GenotypeDepth
all individuals: 171
bin: 1.75e1
variant carriers: 149

GenotypeDepth
all individuals: 2193
bin: 7.25e1
variant carriers: 2004

GenotypeDepth
all individuals: 779
bin: 9.25e1
variant carriers: 672

GenotypeDepth
all individuals: 7420
bin: 9.75e1
variant carriers: 7026

GenotypeDepth
all individuals: 4595
bin: 2.75e1
variant carriers: 1249

GenotypeQuality
all individuals: 21
bin: 2.5e0
variant carriers: 6

GenotypeQuality
all individuals: 129
bin: 5.25e1
variant carriers: 84

GenotypeQuality
all individuals: 798
bin: 7.25e1
variant carriers: 138

GenotypeQuality
all individuals: 16
bin: 7.5e0
variant carriers: 10

GenotypeQuality
all individuals: 21
bin: 1.75e1
variant carriers: 14

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 9

GenotypeQuality
all individuals: 135
bin: 5.75e1
variant carriers: 79

GenotypeQuality
all individuals: 49
bin: 2.25e1
variant carriers: 11

GenotypeQuality
all individuals: 1853
bin: 6.75e1
variant carriers: 177

GenotypeQuality
all individuals: 54
bin: 3.75e1
variant carriers: 27

GenotypeQuality
all individuals: 83
bin: 4.75e1
variant carriers: 50

GenotypeQuality
all individuals: 49214
bin: 9.75e1
variant carriers: 46221

GenotypeQuality
all individuals: 1139
bin: 7.75e1
variant carriers: 222

GenotypeQuality
all individuals: 1025
bin: 8.25e1
variant carriers: 329

GenotypeQuality
all individuals: 59
bin: 4.25e1
variant carriers: 32

GenotypeQuality
all individuals: 57
bin: 2.75e1
variant carriers: 26

GenotypeQuality
all individuals: 4639
bin: 6.25e1
variant carriers: 111

GenotypeQuality
all individuals: 48
bin: 3.25e1
variant carriers: 18

GenotypeQuality
all individuals: 545
bin: 8.75e1
variant carriers: 254

GenotypeQuality
all individuals: 805
bin: 9.25e1
variant carriers: 436

European (Finnish)
type: Population
allele count: 3751
allele frequency: 5.673018753781004e-1
allele num: 6612
num of homozygotes: 1082

South Asian
type: Population
allele count: 7165
allele frequency: 4.342424242424243e-1
allele num: 16500
num of homozygotes: 1615

African
type: Population
allele count: 9005
allele frequency: 8.66198537899192e-1
allele num: 10396
num of homozygotes: 3883

East Asian
type: Population
allele count: 4004
allele frequency: 4.641780663111523e-1
allele num: 8626
num of homozygotes: 925

Latino
type: Population
allele count: 5330
allele frequency: 4.618717504332756e-1
allele num: 11540
num of homozygotes: 1260

Other
type: Population
allele count: 540
allele frequency: 5.973451327433629e-1
allele num: 904
num of homozygotes: 161

European (Non-Finnish)
type: Population
allele count: 38517
allele frequency: 5.778821340694953e-1
allele num: 66652
num of homozygotes: 11176

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.74e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.65e-1

QD
type: SiteQuality
SIO_000300: 2.249e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.53e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.64e0

FS
type: SiteQuality
SIO_000300: 5.46e-1

MQ
type: SiteQuality
SIO_000300: 5.937e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.68e-1

DP
type: SiteQuality
SIO_000300: 3.661955e6

GenotypeDepth
all individuals: 383
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18152
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6155
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 817
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 741
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 995
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1178
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 337
bin: 1.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 86
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 13003
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1314
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2009
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 504
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 628
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3707
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2241
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 62
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3412
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2356
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8424
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1645
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3762
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19584
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4833
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15799
bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500690317546071e-5
allele num: 66636
num of homozygotes: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.841e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.096e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.15e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.68e0

VQSLOD
type: SiteQuality
SIO_000300: -1.563e0

FS
type: SiteQuality
SIO_000300: 9.26e-1

MQ
type: SiteQuality
SIO_000300: 5.703e1

DP
type: SiteQuality
SIO_000300: 2.360302e6

MQRankSum
type: SiteQuality
SIO_000300: -9.340000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10322
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16398
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 7.02e0

VQSLOD
type: SiteQuality
SIO_000300: 4.6e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.34e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.27e-1

DP
type: SiteQuality
SIO_000300: 2.358297e6

MQ
type: SiteQuality
SIO_000300: 5.955e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.44e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.5e-2

GenotypeDepth
all individuals: 1313
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6206
bin: 3.75e1
variant carriers: 5

GenotypeDepth
all individuals: 2007
bin: 9.75e1
variant carriers: 9

GenotypeDepth
all individuals: 6458
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 621
bin: 8.25e1
variant carriers: 2

GenotypeDepth
all individuals: 13043
bin: 3.25e1
variant carriers: 3

GenotypeDepth
all individuals: 94
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 800
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 18088
bin: 2.75e1
variant carriers: 3

GenotypeDepth
all individuals: 377
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 232
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 733
bin: 7.75e1
variant carriers: 1

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

GenotypeDepth
all individuals: 1641
bin: 5.25e1
variant carriers: 2

GenotypeDepth
all individuals: 379
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1157
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3783
bin: 4.25e1
variant carriers: 7

GenotypeQuality
all individuals: 354
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 78
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3292
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3560
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 2.5e0
variant carriers: 0

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

South Asian
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allele count: 15
allele frequency: 9.147457006952067e-4
allele num: 16398
num of homozygotes: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10322
num of homozygotes: 0

Latino
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allele count: 7
allele frequency: 6.090133982947625e-4
allele num: 11494
num of homozygotes: 0

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

East Asian
type: Population
allele count: 6
allele frequency: 6.993006993006993e-4
allele num: 8580
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 17
allele frequency: 2.566347634431328e-4
allele num: 66242
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -8.34e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.5e-2

VQSLOD
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SIO_000300: 4.6e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.44e-2

DP
type: SiteQuality
SIO_000300: 2.358297e6

QD
type: SiteQuality
SIO_000300: 7.02e0

MQ
type: SiteQuality
SIO_000300: 5.955e1

GenotypeDepth
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bin: 7.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 8

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 4

GenotypeDepth
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variant carriers: 4

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 9

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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: 1

African
type: Population
allele count: 2
allele frequency: 1.937608990505716e-4
allele num: 10322
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.219660934260276e-4
allele num: 16398
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.610057421263268e-4
allele num: 11494
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.207693004438272e-4
allele num: 66242
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.165501165501166e-4
allele num: 8580
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.111111111111111e-3
allele num: 900
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: 2.44e-2

ReadPosRankSum
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SIO_000300: 1.6e-2

MQ
type: SiteQuality
SIO_000300: 5.955e1

DP
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SIO_000300: 2.358297e6

ClippingRankSum
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SIO_000300: -7.5e-2

QD
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BaseQRankSum
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SIO_000300: -8.34e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.27e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
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SIO_000300: 4.6e0

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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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 264
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.656509695290859e-5
allele num: 11552
num of homozygotes: 0

Other
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: 8628
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.853e0

BaseQRankSum
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SIO_000300: 2.87e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 2.072e1

ClippingRankSum
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SIO_000300: -1.387e0

ReadPosRankSum
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SIO_000300: 2.97e-1

MQRankSum
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SIO_000300: 1.41e0

FS
type: SiteQuality
SIO_000300: 1.579e0

DP
type: SiteQuality
SIO_000300: 2.319506e6

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
all individuals: 1991
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GenotypeDepth
all individuals: 8
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GenotypeDepth
all individuals: 127
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502087902184036e-5
allele num: 66574
num of homozygotes: 0

Other
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allele count: 0
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.17e-1

VQSLOD
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SIO_000300: -1.765e-1

FS
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SIO_000300: 0.0e0

ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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DP
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MQ
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ClippingRankSum
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SIO_000300: -1.51e-1

QD
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SIO_000300: 1.17e1

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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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: 3

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10374
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6608
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: 3
allele frequency: 3.478664192949907e-4
allele num: 8624
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66566
num of homozygotes: 0

Other
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allele count: 0
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BaseQRankSum
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SIO_000300: -1.735e0

InbreedingCoeff
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DP
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QD
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ReadPosRankSum
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VQSLOD
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FS
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MQRankSum
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MQ
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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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GenotypeDepth
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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: 3.25e1
variant carriers: 0

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

South Asian
type: Population
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allele frequency: 1.819284414796847e-4
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num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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num of homozygotes: 0

Other
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num of homozygotes: 0

QD
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ReadPosRankSum
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InbreedingCoeff
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DP
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FS
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MQ
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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VQSLOD
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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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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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: 6606
num of homozygotes: 0

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

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

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
allele num: 66544
num of homozygotes: 0

African
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allele frequency: 1.929384526336099e-4
allele num: 10366
num of homozygotes: 0

Latino
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allele frequency: 8.664009703690868e-5
allele num: 11542
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DP
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ClippingRankSum
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QD
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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VQSLOD
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MQ
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FS
type: SiteQuality
SIO_000300: 1.335e0

ReadPosRankSum
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SIO_000300: -2.28e-1

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: 1

GenotypeDepth
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variant carriers: 2

GenotypeDepth
all individuals: 1991
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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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GenotypeDepth
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GenotypeDepth
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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 count: 0
allele frequency: 0.0e0
allele num: 904
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: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66494
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

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: 5
allele frequency: 3.034348828741352e-4
allele num: 16478
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.252047e6

MQ
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SIO_000300: 6.039e1

InbreedingCoeff
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SIO_000300: -5.999999999999999e-4

MQRankSum
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VQSLOD
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QD
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FS
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SIO_000300: 2.446e0

ClippingRankSum
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SIO_000300: -8.62e-1

BaseQRankSum
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SIO_000300: 3.58e-1

ReadPosRankSum
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SIO_000300: -7.3e-2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 2

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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variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.507613447911955e-5
allele num: 66330
num of homozygotes: 0

Latino
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allele frequency: 8.679048776254123e-5
allele num: 11522
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: 4
allele frequency: 3.861749372465727e-4
allele num: 10358
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
allele num: 902
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

MQRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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ClippingRankSum
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BaseQRankSum
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QD
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FS
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SIO_000300: 7.32e-1

DP
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ReadPosRankSum
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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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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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66330
num of homozygotes: 0

European (Finnish)
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allele count: 0
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Latino
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allele frequency: 8.679048776254123e-5
allele num: 11522
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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FS
type: SiteQuality
SIO_000300: 7.32e-1

MQRankSum
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QD
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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DP
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InbreedingCoeff
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MQ
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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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GenotypeDepth
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GenotypeDepth
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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: 51

GenotypeQuality
all individuals: 2222
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 35
allele frequency: 5.279671755264587e-4
allele num: 66292
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.108647450110865e-3
allele num: 902
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
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Latino
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allele count: 5
allele frequency: 4.340277777777778e-4
allele num: 11520
num of homozygotes: 0

South Asian
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allele count: 10
allele frequency: 6.076072426783327e-4
allele num: 16458
num of homozygotes: 0

BaseQRankSum
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SIO_000300: 2.99e0

ClippingRankSum
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SIO_000300: 5.5e-2

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

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

European (Non-Finnish)
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South Asian
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African
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Latino
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Other
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East Asian
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FS
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ReadPosRankSum
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DP
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BaseQRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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MQRankSum
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QD
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GenotypeDepth
all individuals: 223
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 20248
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5825
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10251
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 254
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 1.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 3382
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12291
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 263
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2402
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 339
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 651
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1587
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1099
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 298
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 453
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1073
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 3083
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28520
bin: 6.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 15
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4079
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2106
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1384
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 34
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7640
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10928
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2875
bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66722
num of homozygotes: 0

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

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

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.211e1

DP
type: SiteQuality
SIO_000300: 2.096846e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.59e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.56e0

MQRankSum
type: SiteQuality
SIO_000300: 5.29e-1

FS
type: SiteQuality
SIO_000300: 8.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.330000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.41e-1