17-4856157-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856157
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856157
    reference: chr 17
allele count: 6
allele frequency: 6.003001500750375e-5
allele num: 99950
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.153C>T
  hgvsp: ENST00000522249.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.153C>T
  hgvsp: ENST00000519584.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.153C>T
  hgvsp: ENST00000522798.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.153C>T
  hgvsp: ENST00000323997.6:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.153C>T
  hgvsp: ENST00000519602.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.153C>T
  hgvsp: ENST00000522301.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.153C>T
  hgvsp: ENST00000518175.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.219C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.153C>T
  hgvsp: ENST00000520221.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.153C>T
  hgvsp: ENST00000521811.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*99C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.219C>T
  variant of: http://identifiers.org/hgnc/3354
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10265
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8001
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23918
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6405
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4045
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp51Asp
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

17-4856158-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856158
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856158
    reference: chr 17
allele count: 2
allele frequency: 2.001961922684231e-5
allele num: 99902
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*100G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.154G>A
  hgvsp: ENSP00000428811.1:p.Gly52Arg
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.154G>A
  hgvsp: ENSP00000431087.1:p.Gly52Arg
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.154G>A
  hgvsp: ENSP00000324105.6:p.Gly52Arg
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.154G>A
  hgvsp: ENSP00000464874.1:p.Gly52Arg
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.220G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.154G>A
  hgvsp: ENSP00000465697.1:p.Gly52Arg
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.220G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.154G>A
  hgvsp: ENSP00000428502.1:p.Gly52Arg
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.154G>A
  hgvsp: ENSP00000430636.1:p.Gly52Arg
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.154G>A
  hgvsp: ENSP00000467444.1:p.Gly52Arg
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.154G>A
  hgvsp: ENSP00000430055.1:p.Gly52Arg
  variant of: http://identifiers.org/hgnc/3354
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23128
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6330
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10283
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8345
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4536
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly52Arg
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/17-4856160-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856160
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856160
    reference: chr 17
allele count: 1
allele frequency: 9.978048293753741e-6
allele num: 100220
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*102A>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.222A>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.156A>C
  hgvsp: ENST00000519602.1:c.156A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.156A>C
  hgvsp: ENST00000522301.1:c.156A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.156A>C
  hgvsp: ENST00000522798.1:c.156A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.156A>C
  hgvsp: ENST00000518175.1:c.156A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.156A>C
  hgvsp: ENST00000520221.1:c.156A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.156A>C
  hgvsp: ENST00000519584.1:c.156A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.156A>C
  hgvsp: ENST00000521811.1:c.156A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.156A>C
  hgvsp: ENST00000522249.1:c.156A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.156A>C
  hgvsp: ENST00000323997.6:c.156A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.222A>C
  variant of: http://identifiers.org/hgnc/3354
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6347
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23009
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8524
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4599
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly52Gly
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP

17-4856160-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856160
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856159
    reference: chr 17
allele count: 2
allele frequency: 1.995609658750748e-5
allele num: 100220
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.157delG
  hgvsp: ENSP00000428811.1:p.Asp53ThrfsTer11
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.157delG
  hgvsp: ENSP00000428502.1:p.Asp53ThrfsTer11
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.157delG
  hgvsp: ENSP00000467444.1:p.Asp53ThrfsTer11
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.157delG
  hgvsp: ENSP00000430055.1:p.Asp53ThrfsTer11
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.157delG
  hgvsp: ENSP00000431087.1:p.Asp53ThrfsTer11
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.157delG
  hgvsp: ENSP00000324105.6:p.Asp53ThrfsTer11
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.157delG
  hgvsp: ENSP00000430636.1:p.Asp53ThrfsTer57
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*103delG
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.157delG
  hgvsp: ENSP00000464874.1:p.Asp53ThrfsTer11
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.223delG
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.223delG
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.157delG
  hgvsp: ENSP00000465697.1:p.Asp53ThrfsTer11
  variant of: http://identifiers.org/hgnc/3354
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10202
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23009
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6347
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8524
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4599
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp53ThrfsTer11
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: AG
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

http://identifiers.org/exac.variant/17-4856163-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856163
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856163
    reference: chr 17
allele count: 4
allele frequency: 3.994567388351842e-5
allele num: 100136
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.159C>A
  hgvsp: ENSP00000428811.1:p.Asp53Glu
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.159C>A
  hgvsp: ENSP00000465697.1:p.Asp53Glu
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.225C>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.159C>A
  hgvsp: ENSP00000431087.1:p.Asp53Glu
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*105C>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.159C>A
  hgvsp: ENSP00000430055.1:p.Asp53Glu
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.159C>A
  hgvsp: ENSP00000430636.1:p.Asp53Glu
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.159C>A
  hgvsp: ENSP00000428502.1:p.Asp53Glu
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.159C>A
  hgvsp: ENSP00000324105.6:p.Asp53Glu
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.159C>A
  hgvsp: ENSP00000467444.1:p.Asp53Glu
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.225C>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.159C>A
  hgvsp: ENSP00000464874.1:p.Asp53Glu
  variant of: http://identifiers.org/hgnc/3354
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8932
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10151
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22173
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6346
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asp53Glu
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: QD

17-4856170-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856170
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856170
    reference: chr 17
allele count: 4
allele frequency: 3.984857541342897e-5
allele num: 100380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.166C>T
  hgvsp: ENSP00000465697.1:p.Arg56Cys
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.166C>T
  hgvsp: ENSP00000428811.1:p.Arg56Cys
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.166C>T
  hgvsp: ENSP00000464874.1:p.Arg56Cys
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.166C>T
  hgvsp: ENSP00000430055.1:p.Arg56Cys
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.232C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.166C>T
  hgvsp: ENSP00000430636.1:p.Arg56Cys
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.232C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*112C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.166C>T
  hgvsp: ENSP00000428502.1:p.Arg56Cys
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.166C>T
  hgvsp: ENSP00000467444.1:p.Arg56Cys
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.166C>T
  hgvsp: ENSP00000324105.6:p.Arg56Cys
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.166C>T
  hgvsp: ENSP00000431087.1:p.Arg56Cys
  variant of: http://identifiers.org/hgnc/3354
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20747
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9945
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9978
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5865
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6086
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg56Cys
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

17-4856171-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856171
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856171
    reference: chr 17
allele count: 2
allele frequency: 1.993660160689009e-5
allele num: 100318
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.167G>A
  hgvsp: ENSP00000428811.1:p.Arg56His
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.167G>A
  hgvsp: ENSP00000431087.1:p.Arg56His
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.167G>A
  hgvsp: ENSP00000467444.1:p.Arg56His
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.167G>A
  hgvsp: ENSP00000464874.1:p.Arg56His
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.167G>A
  hgvsp: ENSP00000465697.1:p.Arg56His
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.167G>A
  hgvsp: ENSP00000430055.1:p.Arg56His
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.233G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.167G>A
  hgvsp: ENSP00000324105.6:p.Arg56His
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.167G>A
  hgvsp: ENSP00000430636.1:p.Arg56His
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.233G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.167G>A
  hgvsp: ENSP00000428502.1:p.Arg56His
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*113G>A
  variant of: http://identifiers.org/hgnc/3354
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9931
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20339
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6061
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10171
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6090
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg56His
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

17-4856176-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856176
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856176
    reference: chr 17
allele count: 1
allele frequency: 9.920634920634921e-6
allele num: 100800
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.172C>G
  hgvsp: ENSP00000465697.1:p.Leu58Val
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.172C>G
  hgvsp: ENSP00000428502.1:p.Leu58Val
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.172C>G
  hgvsp: ENSP00000324105.6:p.Leu58Val
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.238C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.172C>G
  hgvsp: ENSP00000467444.1:p.Leu58Val
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.172C>G
  hgvsp: ENSP00000431087.1:p.Leu58Val
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.172C>G
  hgvsp: ENSP00000464874.1:p.Leu58Val
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.238C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.172C>G
  hgvsp: ENSP00000428811.1:p.Leu58Val
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.172C>G
  hgvsp: ENSP00000430636.1:p.Leu58Val
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.172C>G
  hgvsp: ENSP00000430055.1:p.Leu58Val
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*118C>G
  variant of: http://identifiers.org/hgnc/3354
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 20145
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6075
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9782
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu58Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum

17-4856181-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856181
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856181
    reference: chr 17
allele count: 1
allele frequency: 9.913357257568848e-6
allele num: 100874
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.177G>A
  hgvsp: ENST00000520221.1:c.177G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.243G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.177G>A
  hgvsp: ENST00000519584.1:c.177G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.177G>A
  hgvsp: ENST00000519602.1:c.177G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.177G>A
  hgvsp: ENST00000522301.1:c.177G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.177G>A
  hgvsp: ENST00000323997.6:c.177G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.177G>A
  hgvsp: ENST00000522798.1:c.177G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.243G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.177G>A
  hgvsp: ENST00000522249.1:c.177G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.177G>A
  hgvsp: ENST00000518175.1:c.177G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.177G>A
  hgvsp: ENST00000521811.1:c.177G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*123G>A
  variant of: http://identifiers.org/hgnc/3354
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6751
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9669
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18857
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11354
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly59Gly
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

17-4856187-TGAG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856187
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856184
    reference: chr 17
allele count: 1
allele frequency: 9.890414210547138e-6
allele num: 101108
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.181+6_181+8delGAG
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.253_255delGAG
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+6_181+8delGAG
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.181+6_181+8delGAG
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.181+6_181+8delGAG
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.181+6_181+8delGAG
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*127+6_*127+8delGAG
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.181+6_181+8delGAG
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.181+6_181+8delGAG
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.247+6_247+8delGAG
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.181+6_181+8delGAG
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.181+6_181+8delGAG
  variant of: http://identifiers.org/hgnc/3354
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11951
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5941
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9439
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7037
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18180
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.181+6_181+8delGAG
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
reference allele: TGAG
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD

17-4856190-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856190
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856190
    reference: chr 17
allele count: 13
allele frequency: 1.284458057504199e-4
allele num: 101210
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.181+5G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.247+5G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.181+5G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.181+5G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*127+5G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+5G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.181+5G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.181+5G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.181+5G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.252G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.181+5G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.181+5G>A
  variant of: http://identifiers.org/hgnc/3354
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12528
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8046
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16654
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5847
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9405
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.181+5G>A
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: African
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/17-4856196-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856196
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856196
    reference: chr 17
allele count: 1
allele frequency: 9.910213465998057e-6
allele num: 100906
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*127+11A>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.258A>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.181+11A>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.181+11A>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.181+11A>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.181+11A>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.181+11A>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.247+11A>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+11A>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.181+11A>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.181+11A>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.181+11A>C
  variant of: http://identifiers.org/hgnc/3354
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5658
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9371
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14893
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9318
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQ

17-4856201-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856201
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856201
    reference: chr 17
allele count: 4
allele frequency: 3.976854705613331e-5
allele num: 100582
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.181+16C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.181+16C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.263C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.181+16C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.181+16C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.181+16C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.181+16C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.181+16C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.181+16C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+16C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.247+16C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*127+16C>T
  variant of: http://identifiers.org/hgnc/3354
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9254
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9999
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14324
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13403
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

17-4856202-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856202
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856202
    reference: chr 17
allele count: 7
allele frequency: 6.988538796373946e-5
allele num: 100164
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.181+17G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.181+17G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.181+17G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.181+17G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.181+17G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.181+17G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.181+17G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*127+17G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+17G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.264G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.247+17G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.181+17G>A
  variant of: http://identifiers.org/hgnc/3354
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13964
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13480
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10296
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9182
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5338
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: FS
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

17-4856202-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856202
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856202
    reference: chr 17
allele count: 2
allele frequency: 1.996725370392556e-5
allele num: 100164
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*127+17G>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.181+17G>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.181+17G>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.181+17G>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.181+17G>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.181+17G>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.181+17G>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.181+17G>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.264G>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+17G>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.181+17G>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.247+17G>C
  variant of: http://identifiers.org/hgnc/3354
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9182
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13480
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10296
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13964
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5338
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/17-4856212-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856212
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856212
    reference: chr 17
allele count: 30
allele frequency: 2.985074626865672e-4
allele num: 100500
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.181+27C>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.247+27C>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*127+27C>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.181+27C>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.181+27C>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.181+27C>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.181+27C>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.181+27C>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.274C>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.181+27C>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+27C>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.181+27C>A
  variant of: http://identifiers.org/hgnc/3354
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13559
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12733
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9134
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11788
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4919
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
reference allele: C
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

17-4856218-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856218
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856218
    reference: chr 17
allele count: 1
allele frequency: 9.925164261468528e-6
allele num: 100754
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*127+33T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.181+33T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.247+33T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.181+33T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.181+33T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.181+33T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.181+33T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+33T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.280T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.181+33T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.181+33T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.181+33T>C
  variant of: http://identifiers.org/hgnc/3354
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4733
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12782
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12132
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13390
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: East Asian
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

17-4856219-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856219
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856219
    reference: chr 17
allele count: 1
allele frequency: 9.934432743890323e-6
allele num: 100660
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.181+34G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.181+34G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.247+34G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.181+34G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.181+34G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.281G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.181+34G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.181+34G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.181+34G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+34G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.181+34G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*127+34G>A
  variant of: http://identifiers.org/hgnc/3354
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9043
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12078
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4773
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12855
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13375
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP

17-4856222-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856222
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856222
    reference: chr 17
allele count: 134
allele frequency: 1.335885472743949e-3
allele num: 100308
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.181+37C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.181+37C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.181+37C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.181+37C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.247+37C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.181+37C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*127+37C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.181+37C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.284C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.181+37C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.181+37C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+37C>T
  variant of: http://identifiers.org/hgnc/3354
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13254
  bin: 1.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 12923
  bin: 2.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 9.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9001
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 12182
  bin: 1.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 3.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
num of homozygotes: 2
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum

17-4856223-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856223
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856223
    reference: chr 17
allele count: 1
allele frequency: 9.915126517014358e-6
allele num: 100856
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.181+38G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+38G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.247+38G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.181+38G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.181+38G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.181+38G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.181+38G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.181+38G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.285G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.181+38G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*127+38G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.181+38G>A
  variant of: http://identifiers.org/hgnc/3354
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13206
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4766
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8951
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13245
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11952
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
population: Latino
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD

17-4856225-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856225
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856225
    reference: chr 17
allele count: 1
allele frequency: 9.877323640386401e-6
allele num: 101242
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.181+40C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.181+40C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.181+40C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.181+40C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.181+40C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.181+40C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*127+40C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.287C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.181+40C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+40C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.181+40C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.247+40C>G
  variant of: http://identifiers.org/hgnc/3354
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4868
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8844
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11683
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13587
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS

17-4856228-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856228
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856228
    reference: chr 17
allele count: 1
allele frequency: 9.824147755182238e-6
allele num: 101790
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.181+43T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.247+43T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.181+43T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.181+43T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.181+43T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.181+43T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.181+43T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.181+43T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.181+43T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+43T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.290T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*127+43T>C
  variant of: http://identifiers.org/hgnc/3354
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8763
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11051
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4900
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12853
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14538
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum

17-4856307-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856307
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856307
    reference: chr 17
allele count: 1
allele frequency: 8.251233559417133e-6
allele num: 121194
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.369G>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+122G>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.248-39G>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.182-39G>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.182-39G>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.182-39G>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.182-39G>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.182-39G>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.182-39G>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*128-39G>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.182-39G>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.182-39G>T
  variant of: http://identifiers.org/hgnc/3354
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6443
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9168
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10357
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6703
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2769
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5584
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4309
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8862
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

17-4856310-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856310
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856310
    reference: chr 17
allele count: 3
allele frequency: 2.474920802534319e-5
allele num: 121216
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.182-36G>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.372G>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.182-36G>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.182-36G>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.182-36G>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.248-36G>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.182-36G>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*128-36G>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+125G>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.182-36G>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.182-36G>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.182-36G>C
  variant of: http://identifiers.org/hgnc/3354
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6707
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6591
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2770
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8945
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9197
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5584
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4311
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10426
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: African
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

17-4856310-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856310
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856310
    reference: chr 17
allele count: 2
allele frequency: 1.649947201689546e-5
allele num: 121216
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.182-36G>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.182-36G>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+125G>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.182-36G>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.182-36G>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.182-36G>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.182-36G>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.248-36G>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.372G>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*128-36G>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.182-36G>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.182-36G>T
  variant of: http://identifiers.org/hgnc/3354
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4311
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9197
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8945
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6591
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10426
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2770
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6707
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

17-4856312-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856312
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856312
    reference: chr 17
allele count: 177
allele frequency: 1.460203273495248e-3
allele num: 121216
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.182-34T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.374T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+127T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.248-34T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*128-34T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.182-34T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.182-34T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.182-34T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.182-34T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.182-34T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.182-34T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.182-34T>C
  variant of: http://identifiers.org/hgnc/3354
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 5.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 7.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10454
  bin: 3.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 5585
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2774
  bin: 5.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8945
  bin: 2.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 4319
  bin: 4.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 6678
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 9200
  bin: 3.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6714
  bin: 4.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 6.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
num of homozygotes: 3
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

17-4856314-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856314
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856314
    reference: chr 17
allele count: 1
allele frequency: 8.249599894405122e-6
allele num: 121218
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.182-32G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.182-32G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*128-32G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.182-32G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.182-32G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+129G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.248-32G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.182-32G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.376G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.182-32G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.182-32G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.182-32G>A
  variant of: http://identifiers.org/hgnc/3354
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2773
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4325
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6709
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10497
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8959
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5586
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6719
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9216
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

17-4856318-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856318
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856318
    reference: chr 17
allele count: 1
allele frequency: 8.247286642694553e-6
allele num: 121252
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.248-28T>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.182-28T>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.182-28T>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.182-28T>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.182-28T>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.182-28T>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.182-28T>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.182-28T>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*128-28T>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.380T>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.182-28T>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+133T>G
  variant of: http://identifiers.org/hgnc/3354
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9238
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6727
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6666
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5586
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2774
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9016
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/17-4856322-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856322
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856322
    reference: chr 17
allele count: 1
allele frequency: 8.24551856066228e-6
allele num: 121278
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.182-24A>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.182-24A>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.248-24A>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.384A>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.182-24A>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.182-24A>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.182-24A>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*128-24A>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.182-24A>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.182-24A>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+137A>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.182-24A>C
  variant of: http://identifiers.org/hgnc/3354
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6669
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10624
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5586
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6737
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4334
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9262
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9049
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD

17-4856330-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856330
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856330
    reference: chr 17
allele count: 7
allele frequency: 5.770911309337334e-5
allele num: 121298
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*128-16C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.182-16C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.182-16C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+145C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.182-16C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.182-16C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.182-16C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.248-16C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.182-16C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.392C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.182-16C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.182-16C>T
  variant of: http://identifiers.org/hgnc/3354
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9095
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4338
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2779
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10680
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6650
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6740
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1621
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5586
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9281
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

17-4856331-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856331
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856331
    reference: chr 17
allele count: 3
allele frequency: 2.473084595980413e-5
allele num: 121306
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.182-15C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+146C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*128-15C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.182-15C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.182-15C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.393C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.182-15C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.182-15C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.182-15C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.248-15C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.182-15C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.182-15C>T
  variant of: http://identifiers.org/hgnc/3354
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2778
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10686
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6651
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1621
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6740
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9284
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5586
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9099
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: C
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

17-4856337-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856337
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856337
    reference: chr 17
allele count: 2
allele frequency: 1.648587160803192e-5
allele num: 121316
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.182-9C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.182-9C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.182-9C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*128-9C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.399C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.182-9C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.182-9C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.182-9C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+152C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.182-9C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.248-9C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.182-9C>G
  variant of: http://identifiers.org/hgnc/3354
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9120
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4341
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10713
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5586
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6627
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9300
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2777
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

17-4856338-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856338
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856338
    reference: chr 17
allele count: 1
allele frequency: 8.242935804015958e-6
allele num: 121316
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.182-8C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.182-8C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*128-8C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.182-8C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.182-8C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.182-8C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.400C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.182-8C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.182-8C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.248-8C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.182-8C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+153C>T
  variant of: http://identifiers.org/hgnc/3354
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5586
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4343
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9122
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6625
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10719
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2778
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.182-8C>T
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

17-4856339-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856339
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856339
    reference: chr 17
allele count: 1
allele frequency: 8.24279991427488e-6
allele num: 121318
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*128-7T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+154T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.182-7T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.182-7T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.182-7T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.182-7T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.182-7T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.182-7T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.401T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.248-7T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.182-7T>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.182-7T>C
  variant of: http://identifiers.org/hgnc/3354
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4342
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9123
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6623
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6748
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5586
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.182-7T>C
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum

17-4856339-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856339
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856339
    reference: chr 17
allele count: 1
allele frequency: 8.24279991427488e-6
allele num: 121318
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.182-7T>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+154T>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.182-7T>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.182-7T>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*128-7T>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.401T>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.248-7T>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.182-7T>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.182-7T>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.182-7T>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.182-7T>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.182-7T>G
  variant of: http://identifiers.org/hgnc/3354
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6623
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6748
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4342
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9298
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10725
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.182-7T>G
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: T
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/17-4856347-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856347
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856347
    reference: chr 17
allele count: 1
allele frequency: 8.241441263248117e-6
allele num: 121338
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.183A>C
  hgvsp: ENST00000323997.6:c.183A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.183A>C
  hgvsp: ENST00000518175.1:c.183A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.183A>C
  hgvsp: ENST00000522798.1:c.183A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.183A>C
  hgvsp: ENST00000521811.1:c.183A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.183A>C
  hgvsp: ENST00000519602.1:c.183A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.409A>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.183A>C
  hgvsp: ENST00000520221.1:c.183A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*129A>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.183A>C
  hgvsp: ENST00000522249.1:c.183A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.249A>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.183A>C
  hgvsp: ENST00000522301.1:c.183A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+162A>C
  variant of: http://identifiers.org/hgnc/3354
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6616
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6754
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4343
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10749
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9307
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.183A>C
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

17-4856350-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856350
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856350
    reference: chr 17
allele count: 4
allele frequency: 3.296413502109704e-5
allele num: 121344
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.186C>T
  hgvsp: ENST00000522249.1:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.186C>T
  hgvsp: ENST00000323997.6:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.186C>T
  hgvsp: ENST00000522798.1:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.186C>T
  hgvsp: ENST00000521811.1:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+165C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.186C>T
  hgvsp: ENST00000518175.1:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.186C>T
  hgvsp: ENST00000522301.1:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.252C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.186C>T
  hgvsp: ENST00000519602.1:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.412C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*132C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.186C>T
  hgvsp: ENST00000520221.1:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9312
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6754
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10750
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9138
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2782
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4343
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6617
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Val62Val
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD

17-4856351-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856351
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856351
    reference: chr 17
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.187C>G
  hgvsp: ENSP00000428811.1:p.Leu63Val
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.187C>G
  hgvsp: ENSP00000428502.1:p.Leu63Val
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.413C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.187C>G
  hgvsp: ENSP00000464874.1:p.Leu63Val
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.187C>G
  hgvsp: ENSP00000467444.1:p.Leu63Val
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.187C>G
  hgvsp: ENSP00000465697.1:p.Leu63Val
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.253C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*133C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.187C>G
  hgvsp: ENSP00000430055.1:p.Leu63Val
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.187C>G
  hgvsp: ENSP00000324105.6:p.Leu63Val
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+166C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.187C>G
  hgvsp: ENSP00000431087.1:p.Leu63Val
  variant of: http://identifiers.org/hgnc/3354
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2784
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9312
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9140
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6616
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6754
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10748
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5586
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4343
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu63Val
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum

17-4856351-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856351
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856351
    reference: chr 17
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.253C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.413C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.187C>T
  hgvsp: ENST00000522798.1:c.187C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.187C>T
  hgvsp: ENST00000323997.6:c.187C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*133C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.187C>T
  hgvsp: ENST00000519602.1:c.187C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.187C>T
  hgvsp: ENST00000520221.1:c.187C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.187C>T
  hgvsp: ENST00000522249.1:c.187C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.187C>T
  hgvsp: ENST00000522301.1:c.187C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.187C>T
  hgvsp: ENST00000521811.1:c.187C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.187C>T
  hgvsp: ENST00000518175.1:c.187C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+166C>T
  variant of: http://identifiers.org/hgnc/3354
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9312
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2784
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4343
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10748
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5586
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6616
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6754
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9140
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu63Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD

17-4856353-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856353
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856353
    reference: chr 17
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.189G>A
  hgvsp: ENST00000522301.1:c.189G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.189G>A
  hgvsp: ENST00000521811.1:c.189G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.189G>A
  hgvsp: ENST00000518175.1:c.189G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.255G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.189G>A
  hgvsp: ENST00000323997.6:c.189G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.189G>A
  hgvsp: ENST00000520221.1:c.189G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.189G>A
  hgvsp: ENST00000522249.1:c.189G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*135G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.415G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.189G>A
  hgvsp: ENST00000519602.1:c.189G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+168G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.189G>A
  hgvsp: ENST00000522798.1:c.189G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4347
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2784
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9312
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6601
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9144
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1631
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6755
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu63Leu
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum

17-4856353-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856353
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856353
    reference: chr 17
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.189G>C
  hgvsp: ENST00000518175.1:c.189G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.189G>C
  hgvsp: ENST00000323997.6:c.189G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.189G>C
  hgvsp: ENST00000520221.1:c.189G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.189G>C
  hgvsp: ENST00000522301.1:c.189G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+168G>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.189G>C
  hgvsp: ENST00000521811.1:c.189G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.189G>C
  hgvsp: ENST00000522249.1:c.189G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*135G>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.255G>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.189G>C
  hgvsp: ENST00000522798.1:c.189G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.189G>C
  hgvsp: ENST00000519602.1:c.189G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.415G>C
  variant of: http://identifiers.org/hgnc/3354
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2784
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1631
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6755
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5586
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6601
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9144
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10753
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu63Leu
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

17-4856357-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856357
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856357
    reference: chr 17
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.193G>C
  hgvsp: ENSP00000465697.1:p.Ala65Pro
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.193G>C
  hgvsp: ENSP00000324105.6:p.Ala65Pro
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.193G>C
  hgvsp: ENSP00000428811.1:p.Ala65Pro
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.193G>C
  hgvsp: ENSP00000430055.1:p.Ala65Pro
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.193G>C
  hgvsp: ENSP00000431087.1:p.Ala65Pro
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.193G>C
  hgvsp: ENSP00000464874.1:p.Ala65Pro
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.259G>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.193G>C
  hgvsp: ENSP00000428502.1:p.Ala65Pro
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*139G>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.419G>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+172G>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.193G>C
  hgvsp: ENSP00000467444.1:p.Ala65Pro
  variant of: http://identifiers.org/hgnc/3354
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6759
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1630
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5586
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9316
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10762
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2785
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9144
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4346
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6591
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala65Pro
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: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ

17-4856365-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856365
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856365
    reference: chr 17
allele count: 8
allele frequency: 6.590871642774756e-5
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.201G>A
  hgvsp: ENST00000522301.1:c.201G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.201G>A
  hgvsp: ENST00000519602.1:c.201G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.201G>A
  hgvsp: ENST00000323997.6:c.201G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.201G>A
  hgvsp: ENST00000518175.1:c.201G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.201G>A
  hgvsp: ENST00000521811.1:c.201G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.201G>A
  hgvsp: ENST00000522798.1:c.201G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.201G>A
  hgvsp: ENST00000522249.1:c.201G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.267G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.427G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*147G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.201G>A
  hgvsp: ENST00000520221.1:c.201G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+180G>A
  variant of: http://identifiers.org/hgnc/3354
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9150
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10771
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6762
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5587
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Glu67Glu
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

http://identifiers.org/exac.variant/17-4856369-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856369
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856369
    reference: chr 17
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.205A>C
  hgvsp: ENSP00000467444.1:p.Ile69Leu
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.205A>C
  hgvsp: ENSP00000465697.1:p.Ile69Leu
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+184A>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.205A>C
  hgvsp: ENSP00000430055.1:p.Ile69Leu
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.431A>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.205A>C
  hgvsp: ENSP00000464874.1:p.Ile69Leu
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*151A>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.205A>C
  hgvsp: ENSP00000324105.6:p.Ile69Leu
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.205A>C
  hgvsp: ENSP00000431087.1:p.Ile69Leu
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.205A>C
  hgvsp: ENSP00000428502.1:p.Ile69Leu
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.205A>C
  hgvsp: ENSP00000428811.1:p.Ile69Leu
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.271A>C
  variant of: http://identifiers.org/hgnc/3354
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5587
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6763
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9317
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10776
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9160
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6551
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4351
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile69Leu
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP

17-4856373-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856373
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856373
    reference: chr 17
allele count: 22
allele frequency: 1.81240011203928e-4
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.209A>G
  hgvsp: ENSP00000324105.6:p.Asn70Ser
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.209A>G
  hgvsp: ENSP00000467444.1:p.Asn70Ser
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.209A>G
  hgvsp: ENSP00000464874.1:p.Asn70Ser
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.275A>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.209A>G
  hgvsp: ENSP00000431087.1:p.Asn70Ser
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.209A>G
  hgvsp: ENSP00000428502.1:p.Asn70Ser
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.209A>G
  hgvsp: ENSP00000428811.1:p.Asn70Ser
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.209A>G
  hgvsp: ENSP00000465697.1:p.Asn70Ser
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.209A>G
  hgvsp: ENSP00000430055.1:p.Asn70Ser
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*155A>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+188A>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.435A>G
  variant of: http://identifiers.org/hgnc/3354
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9164
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5592
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9315
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6538
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2787
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6764
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4353
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asn70Ser
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

17-4856375-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856375
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856375
    reference: chr 17
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.211A>G
  hgvsp: ENSP00000467444.1:p.Asn71Asp
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*157A>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.437A>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.211A>G
  hgvsp: ENSP00000428811.1:p.Asn71Asp
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.211A>G
  hgvsp: ENSP00000428502.1:p.Asn71Asp
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.211A>G
  hgvsp: ENSP00000430055.1:p.Asn71Asp
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.211A>G
  hgvsp: ENSP00000465697.1:p.Asn71Asp
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.211A>G
  hgvsp: ENSP00000464874.1:p.Asn71Asp
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.211A>G
  hgvsp: ENSP00000324105.6:p.Asn71Asp
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.277A>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+190A>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.211A>G
  hgvsp: ENSP00000431087.1:p.Asn71Asp
  variant of: http://identifiers.org/hgnc/3354
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2788
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5592
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6763
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9169
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9317
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10782
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4354
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn71Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

17-4856376-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856376
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856376
    reference: chr 17
allele count: 78777
allele frequency: 6.49278826341383e-1
allele num: 121330
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.212A>G
  hgvsp: ENSP00000431087.1:p.Asn71Ser
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.438A>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.212A>G
  hgvsp: ENSP00000324105.6:p.Asn71Ser
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.212A>G
  hgvsp: ENSP00000428811.1:p.Asn71Ser
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.212A>G
  hgvsp: ENSP00000464874.1:p.Asn71Ser
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.212A>G
  hgvsp: ENSP00000428502.1:p.Asn71Ser
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.278A>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*158A>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.212A>G
  hgvsp: ENSP00000465697.1:p.Asn71Ser
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.212A>G
  hgvsp: ENSP00000430055.1:p.Asn71Ser
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+191A>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.212A>G
  hgvsp: ENSP00000467444.1:p.Asn71Ser
  variant of: http://identifiers.org/hgnc/3354
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4383
  bin: 6.25e1
  variant carriers: 4275
genotype depth: GenotypeDepth
  all individuals: 3590
  bin: 8.25e1
  variant carriers: 3544
genotype depth: GenotypeDepth
  all individuals: 2130
  bin: 4.25e1
  variant carriers: 1371
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 2497
  bin: 4.75e1
  variant carriers: 2078
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 2.25e1
  variant carriers: 115
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 3238
  bin: 5.25e1
  variant carriers: 2966
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 2.75e1
  variant carriers: 243
genotype depth: GenotypeDepth
  all individuals: 4687
  bin: 7.25e1
  variant carriers: 4630
genotype depth: GenotypeDepth
  all individuals: 4635
  bin: 6.75e1
  variant carriers: 4527
genotype depth: GenotypeDepth
  all individuals: 3946
  bin: 5.75e1
  variant carriers: 3732
genotype depth: GenotypeDepth
  all individuals: 14744
  bin: 9.75e1
  variant carriers: 13737
genotype depth: GenotypeDepth
  all individuals: 2623
  bin: 9.25e1
  variant carriers: 2552
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 3.75e1
  variant carriers: 814
genotype quality: GenotypeQuality
hgvs: p.Asn71Ser
num of homozygotes: 26298
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP

17-4856381-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856381
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856381
    reference: chr 17
allele count: 2
allele frequency: 1.647419317638919e-5
allele num: 121402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.217C>G
  hgvsp: ENSP00000465697.1:p.Leu73Val
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.443C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+196C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.217C>G
  hgvsp: ENSP00000467444.1:p.Leu73Val
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.217C>G
  hgvsp: ENSP00000428502.1:p.Leu73Val
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.283C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.217C>G
  hgvsp: ENSP00000464874.1:p.Leu73Val
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.217C>G
  hgvsp: ENSP00000431087.1:p.Leu73Val
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.217C>G
  hgvsp: ENSP00000324105.6:p.Leu73Val
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*163C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.217C>G
  hgvsp: ENSP00000430055.1:p.Leu73Val
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.217C>G
  hgvsp: ENSP00000428811.1:p.Leu73Val
  variant of: http://identifiers.org/hgnc/3354
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9185
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2938
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4563
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3869
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3945
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4547
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4972
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5492
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu73Val
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD

17-4856390-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856390
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856390
    reference: chr 17
allele count: 237
allele frequency: 1.952224052718287e-3
allele num: 121400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.226G>C
  hgvsp: ENSP00000465697.1:p.Ala76Pro
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.226G>C
  hgvsp: ENSP00000467444.1:p.Ala76Pro
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.226G>C
  hgvsp: ENSP00000428502.1:p.Ala76Pro
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.226G>C
  hgvsp: ENSP00000324105.6:p.Ala76Pro
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*172G>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.226G>C
  hgvsp: ENSP00000428811.1:p.Ala76Pro
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.226G>C
  hgvsp: ENSP00000464874.1:p.Ala76Pro
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.452G>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.226G>C
  hgvsp: ENSP00000430055.1:p.Ala76Pro
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+205G>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.292G>C
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.226G>C
  hgvsp: ENSP00000431087.1:p.Ala76Pro
  variant of: http://identifiers.org/hgnc/3354
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3954
  bin: 7.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 4573
  bin: 6.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3171
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1898
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2911
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4985
  bin: 5.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 5310
  bin: 6.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 9.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3142
  bin: 7.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 4555
  bin: 4.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 2287
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 8.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
hgvs: p.Ala76Pro
num of homozygotes: 2
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

17-4856392-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856392
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856392
    reference: chr 17
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.228T>G
  hgvsp: ENST00000522798.1:c.228T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.228T>G
  hgvsp: ENST00000520221.1:c.228T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.454T>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.228T>G
  hgvsp: ENST00000521811.1:c.228T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.228T>G
  hgvsp: ENST00000522301.1:c.228T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.228T>G
  hgvsp: ENST00000522249.1:c.228T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.228T>G
  hgvsp: ENST00000518175.1:c.228T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.228T>G
  hgvsp: ENST00000519602.1:c.228T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.294T>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*174T>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+207T>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.228T>G
  hgvsp: ENST00000323997.6:c.228T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3354
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5505
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4985
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2297
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4556
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5310
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4564
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2916
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3945
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3175
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala76Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum

17-4856399-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856399
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856399
    reference: chr 17
allele count: 3
allele frequency: 2.471251112063001e-5
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*181C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.301C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.235C>T
  hgvsp: ENSP00000431087.1:p.Gln79Ter
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.461C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.235C>T
  hgvsp: ENSP00000464874.1:p.Gln79Ter
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.235C>T
  hgvsp: ENSP00000465697.1:p.Gln79Ter
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.235C>T
  hgvsp: ENSP00000428811.1:p.Gln79Ter
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.235C>T
  hgvsp: ENSP00000430055.1:p.Gln79Ter
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.235C>T
  hgvsp: ENSP00000428502.1:p.Gln79Ter
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.235C>T
  hgvsp: ENSP00000324105.6:p.Gln79Ter
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.235C>T
  hgvsp: ENSP00000467444.1:p.Gln79Ter
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+214C>T
  variant of: http://identifiers.org/hgnc/3354
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2295
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3946
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2922
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2457
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4561
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5311
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5505
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3896
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3176
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3141
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gln79Ter
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD

17-4856402-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856402
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856402
    reference: chr 17
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.238A>T
  hgvsp: ENSP00000428811.1:p.Lys80Ter
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.238A>T
  hgvsp: ENSP00000324105.6:p.Lys80Ter
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.238A>T
  hgvsp: ENSP00000467444.1:p.Lys80Ter
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.238A>T
  hgvsp: ENSP00000464874.1:p.Lys80Ter
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.464A>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+217A>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.238A>T
  hgvsp: ENSP00000430055.1:p.Lys80Ter
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*184A>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.238A>T
  hgvsp: ENSP00000465697.1:p.Lys80Ter
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.304A>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.238A>T
  hgvsp: ENSP00000428502.1:p.Lys80Ter
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.238A>T
  hgvsp: ENSP00000431087.1:p.Lys80Ter
  variant of: http://identifiers.org/hgnc/3354
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4558
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2458
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3171
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5311
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3896
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3946
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1898
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3141
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys80Ter
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD

17-4856412-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856412
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856412
    reference: chr 17
allele count: 3
allele frequency: 2.47133254250692e-5
allele num: 121392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.240+8G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.240+8G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.240+8G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.240+8G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.306+8G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.240+8G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.240+8G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*186+8G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.240+8G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.474G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+227G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.240+8G>A
  variant of: http://identifiers.org/hgnc/3354
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2921
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3901
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3161
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2457
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4557
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5311
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4562
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4990
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.240+8G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP

17-4856421-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856421
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856421
    reference: chr 17
allele count: 1013
allele frequency: 8.345691217663535e-3
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.240+17G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.240+17G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.240+17G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.240+17G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.240+17G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.240+17G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+236G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.483G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.306+17G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.240+17G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*186+17G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.240+17G>A
  variant of: http://identifiers.org/hgnc/3354
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2815
  bin: 3.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 3171
  bin: 7.75e1
  variant carriers: 64
genotype depth: GenotypeDepth
  all individuals: 5330
  bin: 6.25e1
  variant carriers: 94
genotype depth: GenotypeDepth
  all individuals: 2176
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5523
  bin: 5.75e1
  variant carriers: 79
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3888
  bin: 4.25e1
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2482
  bin: 8.25e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 5015
  bin: 5.25e1
  variant carriers: 90
genotype depth: GenotypeDepth
  all individuals: 3990
  bin: 7.25e1
  variant carriers: 86
genotype depth: GenotypeDepth
  all individuals: 4551
  bin: 4.75e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 8.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 4589
  bin: 6.75e1
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 9234
  bin: 9.75e1
  variant carriers: 171
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3090
  bin: 3.75e1
  variant carriers: 33
genotype quality: GenotypeQuality
num of homozygotes: 39
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/17-4856424-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856424
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856424
    reference: chr 17
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.486C>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.306+20C>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.240+20C>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.240+20C>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.240+20C>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.240+20C>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+239C>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.240+20C>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*186+20C>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.240+20C>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.240+20C>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.240+20C>A
  variant of: http://identifiers.org/hgnc/3354
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2175
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3968
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3890
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5323
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2479
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5016
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3110
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9207
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2818
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4589
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4578
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

17-4856424-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856424
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856424
    reference: chr 17
allele count: 6
allele frequency: 4.943316635908252e-5
allele num: 121376
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.240+20C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*186+20C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.240+20C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.486C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.240+20C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.240+20C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.240+20C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.240+20C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.240+20C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.306+20C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+239C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.240+20C>T
  variant of: http://identifiers.org/hgnc/3354
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2175
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3167
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3110
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4589
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5016
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5323
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4578
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9207
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2818
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2479
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3890
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD

17-4856425-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856425
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856425
    reference: chr 17
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.240+21G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.240+21G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.240+21G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.240+21G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.240+21G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*186+21G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.487G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.240+21G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.240+21G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.306+21G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.240+21G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+240G>A
  variant of: http://identifiers.org/hgnc/3354
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5525
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3166
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5022
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3968
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5324
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2176
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4587
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3107
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2481
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9207
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/17-4856429-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856429
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856430
    reference: chr 17
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.306+26dupA
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.240+26dupA
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.492dupA
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.240+26dupA
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.240+26dupA
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.240+26dupA
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.240+26dupA
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+245dupA
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.240+26dupA
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.240+26dupA
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*186+26dupA
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.240+26dupA
  variant of: http://identifiers.org/hgnc/3354
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4586
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4576
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3112
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3888
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2154
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9207
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2482
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2802
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5323
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5522
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5026
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3167
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

17-4856430-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856430
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856430
    reference: chr 17
allele count: 29
allele frequency: 2.389348449395248e-4
allele num: 121372
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.240+26A>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.240+26A>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.240+26A>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.492A>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.240+26A>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.240+26A>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.240+26A>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.306+26A>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.240+26A>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.240+26A>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+245A>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*186+26A>G
  variant of: http://identifiers.org/hgnc/3354
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3877
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2148
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4577
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5029
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3168
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2798
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3114
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5523
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2485
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 9207
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5327
  bin: 6.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: A
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

17-4856431-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856431
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856431
    reference: chr 17
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.306+27G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.240+27G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.240+27G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.240+27G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*186+27G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+246G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.493G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.240+27G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.240+27G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.240+27G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.240+27G>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.240+27G>A
  variant of: http://identifiers.org/hgnc/3354
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3877
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2486
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4589
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5327
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9207
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3114
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2792
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4576
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

17-4856433-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856433
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856433
    reference: chr 17
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.240+29C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.240+29C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.495C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+248C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.240+29C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.240+29C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.240+29C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.306+29C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.240+29C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.240+29C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.240+29C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*186+29C>T
  variant of: http://identifiers.org/hgnc/3354
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3113
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9207
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4578
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4588
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2148
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5031
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3877
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5329
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5522
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2788
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2487
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3167
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
reference allele: C
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

17-4856438-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856438
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856438
    reference: chr 17
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.240+34C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.240+34C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.240+34C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*186+34C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.240+34C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.500C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.240+34C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.240+34C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.306+34C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.240+34C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+253C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.240+34C>T
  variant of: http://identifiers.org/hgnc/3354
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4587
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5033
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4578
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9207
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5329
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2134
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3875
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3110
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2768
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2487
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD

17-4856447-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856447
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856447
    reference: chr 17
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*186+43C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.240+43C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.240+43C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.240+43C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.509C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.306+43C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.240+43C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.240+43C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.240+43C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+262C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.240+43C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.240+43C>T
  variant of: http://identifiers.org/hgnc/3354
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3117
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2764
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3877
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5534
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9207
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2077
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4578
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2488
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4588
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/17-4856448-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856448
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856448
    reference: chr 17
allele count: 3
allele frequency: 2.471780505891077e-5
allele num: 121370
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.240+44C>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.240+44C>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.240+44C>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*186+44C>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.240+44C>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.306+44C>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+263C>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.240+44C>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.510C>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.240+44C>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.240+44C>A
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.240+44C>A
  variant of: http://identifiers.org/hgnc/3354
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2487
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5330
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4576
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4590
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5536
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2078
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3878
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3115
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2765
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5038
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

17-4856448-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856448
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856448
    reference: chr 17
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.240+44C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.510C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.240+44C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.240+44C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*186+44C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.240+44C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+263C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.240+44C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.240+44C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.306+44C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.240+44C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.240+44C>T
  variant of: http://identifiers.org/hgnc/3354
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2487
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9207
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5536
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2078
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5330
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3878
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5038
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4576
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2765
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3115
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP

17-4856451-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856451
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856451
    reference: chr 17
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.240+47C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.513C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.240+47C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.306+47C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+266C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.240+47C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.240+47C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.240+47C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.240+47C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.240+47C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*186+47C>G
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.240+47C>G
  variant of: http://identifiers.org/hgnc/3354
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2769
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4574
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3881
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9207
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5037
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3112
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5333
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5540
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2487
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4589
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

17-4856454-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4856454
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4856454
    reference: chr 17
allele count: 2
allele frequency: 1.647880825258717e-5
allele num: 121368
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000571235
  gene symbol: ENO3
  hgvsc: ENST00000571235.1:n.516C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000467444
  ensembl transcript: ENST00000520221
  gene symbol: ENO3
  hgvsc: ENST00000520221.1:c.240+50C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430055
  ensembl transcript: ENST00000519602
  gene symbol: ENO3
  hgvsc: ENST00000519602.1:c.240+50C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428811
  ensembl transcript: ENST00000522249
  gene symbol: ENO3
  hgvsc: ENST00000522249.1:c.240+50C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000324105
  ensembl transcript: ENST00000323997
  gene symbol: ENO3
  hgvsc: ENST00000323997.6:c.240+50C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000431087
  ensembl transcript: ENST00000518175
  gene symbol: ENO3
  hgvsc: ENST00000518175.1:c.240+50C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430636
  ensembl transcript: ENST00000519584
  gene symbol: ENO3
  hgvsc: ENST00000519584.1:c.181+269C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000428502
  ensembl transcript: ENST00000522798
  gene symbol: ENO3
  hgvsc: ENST00000522798.1:c.240+50C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000464874
  ensembl transcript: ENST00000521811
  gene symbol: ENO3
  hgvsc: ENST00000521811.1:c.240+50C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000465697
  ensembl transcript: ENST00000522301
  gene symbol: ENO3
  hgvsc: ENST00000522301.1:c.240+50C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl protein: ENSP00000430554
  ensembl transcript: ENST00000521659
  gene symbol: ENO3
  hgvsc: ENST00000521659.1:c.*186+50C>T
  variant of: http://identifiers.org/hgnc/3354
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108515
  ensembl transcript: ENST00000519834
  gene symbol: ENO3
  hgvsc: ENST00000519834.1:n.306+50C>T
  variant of: http://identifiers.org/hgnc/3354
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5336
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2077
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2769
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5037
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5539
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2488
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3112
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4590
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3885
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4572
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
reference allele: C

GenotypeDepth
all individuals: 1165
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 451
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 535
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 984
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13483
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2511
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2900
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 659
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 991
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6098
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 661
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1766
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2233
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25967
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 584
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 417
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 1.053296819043606e-4
allele num: 9494
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 740
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7520
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.940588561910051e-5
allele num: 14408
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.105263157894737e-4
allele num: 4750
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.494505494505495e-5
allele num: 54600
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8438
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.1e0

FS
type: SiteQuality
SIO_000300: 5.679999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.98e-1

QD
type: SiteQuality
SIO_000300: 1.129e1

MQRankSum
type: SiteQuality
SIO_000300: 3.68e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.37e0

DP
type: SiteQuality
SIO_000300: 1.459695e6

GenotypeDepth
all individuals: 344
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 534
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 467
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1265
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2672
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1104
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1904
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 851
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6094
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 13662
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3071
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2203
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 24420
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 576
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 658
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 713
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9490
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4774
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 740
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.832978957401569e-5
allele num: 54556
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.938662225922843e-5
allele num: 14412
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8412
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7518
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.453221e6

BaseQRankSum
type: SiteQuality
SIO_000300: 8.149999999999999e-1

FS
type: SiteQuality
SIO_000300: 4.2e-1

MQ
type: SiteQuality
SIO_000300: 5.954e1

QD
type: SiteQuality
SIO_000300: 1.07e1

VQSLOD
type: SiteQuality
SIO_000300: 6.62e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.77e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.2e-2

GenotypeDepth
all individuals: 408
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10202
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 503
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 657
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 499
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 697
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1902
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13714
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2700
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1138
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 582
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1084
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2236
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3121
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6094
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 24877
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54742
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9524
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8456
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 742
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4782
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.923289947382996e-5
allele num: 14444
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.315e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.56e-1

FS
type: SiteQuality
SIO_000300: 4.319e0

MQ
type: SiteQuality
SIO_000300: 5.913e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 9.59e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.81e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.024e0

QD
type: SiteQuality
SIO_000300: 1.36e1

DP
type: SiteQuality
SIO_000300: 1.451845e6

GenotypeDepth
all individuals: 540
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 579
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 503
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 582
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2236
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 657
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13714
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3121
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1084
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2700
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 499
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 697
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele frequency: 3.653501881553469e-5
allele num: 54742
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

DP
type: SiteQuality
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VQSLOD
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MQ
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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FS
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: 1.8e-3

QD
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GenotypeDepth
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GenotypeDepth
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variant carriers: 1

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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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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East Asian
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allele frequency: 3.996802557953637e-4
allele num: 7506
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European (Non-Finnish)
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allele frequency: 1.829625292740047e-5
allele num: 54656
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VQSLOD
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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DP
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FS
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Finnish)
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allele frequency: 0.0e0
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Latino
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South Asian
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Other
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European (Non-Finnish)
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allele frequency: 3.650434401693802e-5
allele num: 54788
num of homozygotes: 0

African
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ClippingRankSum
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FS
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DP
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MQRankSum
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InbreedingCoeff
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MQ
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QD
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ReadPosRankSum
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VQSLOD
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SIO_000300: 8.68e-1

BaseQRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7488
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.650834215618269e-5
allele num: 54782
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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South Asian
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QD
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DP
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VQSLOD
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InbreedingCoeff
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MQRankSum
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FS
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ReadPosRankSum
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ClippingRankSum
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SIO_000300: -1.9e-1

MQ
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BaseQRankSum
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SIO_000300: 6.78e-1

GenotypeDepth
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variant carriers: 0

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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allele frequency: 1.177024482109228e-4
allele num: 8496
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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Latino
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East Asian
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Other
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European (Non-Finnish)
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South Asian
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InbreedingCoeff
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MQRankSum
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DP
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ClippingRankSum
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BaseQRankSum
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MQ
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VQSLOD
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QD
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FS
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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Latino
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Other
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East Asian
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African
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South Asian
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ReadPosRankSum
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InbreedingCoeff
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DP
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MQ
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FS
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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QD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Other
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Latino
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European (Non-Finnish)
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East Asian
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South Asian
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African
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BaseQRankSum
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MQ
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ReadPosRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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FS
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DP
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QD
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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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bin: 9.25e1
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GenotypeQuality
all individuals: 6099
bin: 9.75e1
variant carriers: 13

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5098
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 7412
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 13
allele frequency: 2.35072872590503e-4
allele num: 55302
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9554
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 748
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 3.89e0

DP
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SIO_000300: 1.401524e6

MQRankSum
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SIO_000300: -2.9e-2

QD
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

ReadPosRankSum
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SIO_000300: 3.26e-1

BaseQRankSum
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SIO_000300: -1.106e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.947e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.44e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7348
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14600
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8450
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.814355178169679e-5
allele num: 55116
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.82e-1

BaseQRankSum
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SIO_000300: 1.13e0

InbreedingCoeff
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QD
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ReadPosRankSum
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VQSLOD
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DP
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SIO_000300: 1.386498e6

FS
type: SiteQuality
SIO_000300: 2.005e0

ClippingRankSum
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SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.915e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9420
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8414
num of homozygotes: 0

East Asian
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allele count: 2
allele frequency: 2.74423710208562e-4
allele num: 7288
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 (Finnish)
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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: 2
allele frequency: 3.638083457634518e-5
allele num: 54974
num of homozygotes: 0

Other
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MQRankSum
type: SiteQuality
SIO_000300: 4.56e-1

BaseQRankSum
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SIO_000300: -6.36e-1

MQ
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SIO_000300: 6.0e1

ClippingRankSum
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DP
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InbreedingCoeff
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SIO_000300: -3.6e-3

FS
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SIO_000300: 4.478e0

QD
type: SiteQuality
SIO_000300: 8.529999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

ReadPosRankSum
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SIO_000300: 2.28e-1

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 14146
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9410
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8372
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5140
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.846501437765302e-5
allele num: 14606
num of homozygotes: 0

European (Non-Finnish)
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allele count: 5
allele frequency: 9.148126463700235e-5
allele num: 54656
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.380452788514633e-4
allele num: 7244
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.324e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
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ClippingRankSum
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InbreedingCoeff
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SIO_000300: 3.5e-3

ReadPosRankSum
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QD
type: SiteQuality
SIO_000300: 9.710000000000001e0

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 1.74e0

BaseQRankSum
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SIO_000300: -1.249e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 2

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14606
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.659250585480094e-5
allele num: 54656
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8372
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9410
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 5140
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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MQ
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VQSLOD
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FS
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BaseQRankSum
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ReadPosRankSum
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QD
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DP
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SIO_000300: 1.378482e6

GenotypeDepth
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variant carriers: 1

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14648
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele frequency: 0.0e0
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European (Finnish)
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African
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allele frequency: 3.556187766714083e-3
allele num: 8436
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East Asian
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MQ
type: SiteQuality
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DP
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ClippingRankSum
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VQSLOD
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FS
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QD
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 744
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9388
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 54960
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8440
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.40331181588549e-4
allele num: 7126
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.586e1

InbreedingCoeff
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MQ
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SIO_000300: 5.922e1

ReadPosRankSum
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SIO_000300: 5.94e-1

BaseQRankSum
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ClippingRankSum
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SIO_000300: -7.6e-1

VQSLOD
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SIO_000300: -1.094e-1

FS
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SIO_000300: 4.52e0

MQRankSum
type: SiteQuality
SIO_000300: 8.94e-1

DP
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SIO_000300: 1.367409e6

GenotypeDepth
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variant carriers: 12

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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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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variant carriers: 129

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2

Other
type: Population
allele count: 1
allele frequency: 1.358695652173913e-3
allele num: 736
num of homozygotes: 0

African
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allele count: 2
allele frequency: 2.378686964795433e-4
allele num: 8408
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9302
num of homozygotes: 0

European (Finnish)
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allele count: 7
allele frequency: 1.31184407796102e-3
allele num: 5336
num of homozygotes: 0

South Asian
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allele count: 123
allele frequency: 8.386744852038729e-3
allele num: 14666
num of homozygotes: 2

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7086
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.825683718552598e-5
allele num: 54774
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
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SIO_000300: 5.95e0

InbreedingCoeff
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SIO_000300: 2.5e-3

ReadPosRankSum
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FS
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QD
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DP
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ClippingRankSum
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SIO_000300: -1.97e-1

BaseQRankSum
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SIO_000300: 1.33e-1

MQRankSum
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SIO_000300: 2.04e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7094
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55108
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5374
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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num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 748
num of homozygotes: 0

Latino
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allele frequency: 1.066325442525059e-4
allele num: 9378
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VQSLOD
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FS
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SIO_000300: 1.387e0

DP
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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SIO_000300: -1.2e-3

BaseQRankSum
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SIO_000300: 6.53e-1

MQ
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SIO_000300: 6.0e1

QD
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SIO_000300: 1.793e1

GenotypeDepth
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 746
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.806554178559815e-5
allele num: 55354
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5404
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
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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

African
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.048e0

ClippingRankSum
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SIO_000300: -1.73e-1

DP
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SIO_000300: 1.378113e6

ReadPosRankSum
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MQ
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SIO_000300: 5.933e1

VQSLOD
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QD
type: SiteQuality
SIO_000300: 1.687e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 8.64e-1

FS
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SIO_000300: 0.0e0

GenotypeDepth
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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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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.796816041973623e-5
allele num: 55654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8528
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 756
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9454
num of homozygotes: 0

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

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

East Asian
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allele frequency: 0.0e0
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ClippingRankSum
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SIO_000300: -1.89e-1

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10366
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

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

European (Finnish)
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East Asian
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num of homozygotes: 0

South Asian
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QD
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FS
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DP
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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MQ
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

European (Finnish)
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East Asian
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Other
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African
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allele num: 10370
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MQRankSum
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DP
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MQ
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QD
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InbreedingCoeff
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ReadPosRankSum
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FS
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.00048007681229e-5
allele num: 66656
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 2.810624e6

MQ
type: SiteQuality
SIO_000300: 5.962e1

FS
type: SiteQuality
SIO_000300: 3.756e0

VQSLOD
type: SiteQuality
SIO_000300: 1.75e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.89e-1

QD
type: SiteQuality
SIO_000300: 1.481e1

MQRankSum
type: SiteQuality
SIO_000300: 1.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.062e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.18e-1

GenotypeDepth
all individuals: 527
bin: 7.25e1
variant carriers: 6

GenotypeQuality
all individuals: 90
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4323
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4060
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
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GenotypeQuality
all individuals: 6772
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 4531
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4404
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GenotypeQuality
all individuals: 30313
bin: 9.75e1
variant carriers: 174

African
type: Population
allele count: 162
allele frequency: 1.5625e-2
allele num: 10368
num of homozygotes: 3

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

Other
type: Population
allele count: 1
allele frequency: 1.103752759381898e-3
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.000570108320581e-5
allele num: 66654
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

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

Latino
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allele count: 12
allele frequency: 1.038961038961039e-3
allele num: 11550
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.79e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.76e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.54e0

QD
type: SiteQuality
SIO_000300: 1.471e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.76e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.43e0

DP
type: SiteQuality
SIO_000300: 2.814205e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.85e-1

GenotypeDepth
all individuals: 407
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4341
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 136
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variant carriers: 0

GenotypeQuality
all individuals: 6
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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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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2650
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variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 5.25e1
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: 10370
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500420117632937e-5
allele num: 66648
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.54e0

FS
type: SiteQuality
SIO_000300: 1.393e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.545e0

MQRankSum
type: SiteQuality
SIO_000300: -1.96e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.712e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 2.816013e6

QD
type: SiteQuality
SIO_000300: 1.653e1

GenotypeDepth
all individuals: 10587
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 56
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variant carriers: 0

GenotypeQuality
all individuals: 109
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variant carriers: 0

GenotypeQuality
all individuals: 4461
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 4362
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 37
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variant carriers: 0

GenotypeQuality
all individuals: 6812
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4098
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 30317
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variant carriers: 1

GenotypeQuality
all individuals: 2768
bin: 7.25e1
variant carriers: 0

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

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66670
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.32e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.08e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.259e0

DP
type: SiteQuality
SIO_000300: 2.818951e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.4e-2

MQ
type: SiteQuality
SIO_000300: 5.916e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.2e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.841e-1

GenotypeDepth
all individuals: 333
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 48
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variant carriers: 0

GenotypeQuality
all individuals: 64
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variant carriers: 0

GenotypeQuality
all individuals: 81
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variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 86
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GenotypeQuality
all individuals: 4108
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variant carriers: 0

GenotypeQuality
all individuals: 30338
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variant carriers: 1

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 2698
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 28
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variant carriers: 0

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 4371
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variant carriers: 0

GenotypeQuality
all individuals: 6840
bin: 6.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.63948332369385e-5
allele num: 10374
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66680
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
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: 6612
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.63e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.22e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

DP
type: SiteQuality
SIO_000300: 2.821197e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.79e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.840000000000001e-1

FS
type: SiteQuality
SIO_000300: 3.204e0

QD
type: SiteQuality
SIO_000300: 1.539e1

GenotypeDepth
all individuals: 983
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 35
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 24
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GenotypeQuality
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GenotypeQuality
all individuals: 4117
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GenotypeQuality
all individuals: 28
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GenotypeQuality
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GenotypeQuality
all individuals: 56
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GenotypeQuality
all individuals: 4
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GenotypeQuality
all individuals: 6851
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 71
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variant carriers: 0

GenotypeQuality
all individuals: 2812
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30355
bin: 9.75e1
variant carriers: 7

Latino
type: Population
allele count: 3
allele frequency: 2.595155709342561e-4
allele num: 11560
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: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 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: 4
allele frequency: 5.99790073474284e-5
allele num: 66690
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.159e1

MQ
type: SiteQuality
SIO_000300: 5.966e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.984e0

MQRankSum
type: SiteQuality
SIO_000300: 2.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.12e-1

DP
type: SiteQuality
SIO_000300: 2.823454e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.03e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.99e-1

GenotypeDepth
all individuals: 4339
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variant carriers: 0

GenotypeQuality
all individuals: 43
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GenotypeQuality
all individuals: 4514
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 21
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variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 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: 16504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.498155756139982e-5
allele num: 66694
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: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
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FS
type: SiteQuality
SIO_000300: 1.14e0

MQ
type: SiteQuality
SIO_000300: 5.916e1

MQRankSum
type: SiteQuality
SIO_000300: 5.85e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.42e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.46e-1

DP
type: SiteQuality
SIO_000300: 2.823747e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.53e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e0

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 3.0e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2826
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 6844
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 3.75e1
variant carriers: 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: 6612
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.211827435773146e-4
allele num: 16504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66700
num of homozygotes: 0

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

Other
type: Population
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.92e0

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.26e-2

FS
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QD
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DP
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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num of homozygotes: 0

European (Non-Finnish)
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East Asian
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European (Finnish)
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South Asian
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African
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Other
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DP
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QD
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BaseQRankSum
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FS
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MQ
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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East Asian
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African
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European (Finnish)
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European (Non-Finnish)
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VQSLOD
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DP
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BaseQRankSum
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MQRankSum
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QD
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ClippingRankSum
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InbreedingCoeff
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MQ
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FS
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Non-Finnish)
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Latino
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South Asian
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African
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European (Finnish)
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FS
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ReadPosRankSum
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InbreedingCoeff
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DP
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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MQ
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QD
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VQSLOD
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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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European (Finnish)
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Latino
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African
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South Asian
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European (Non-Finnish)
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QD
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ClippingRankSum
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InbreedingCoeff
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MQ
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VQSLOD
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BaseQRankSum
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FS
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ReadPosRankSum
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DP
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MQRankSum
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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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Latino
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European (Finnish)
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South Asian
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African
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.498980693128672e-5
allele num: 66712
num of homozygotes: 0

MQRankSum
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MQ
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FS
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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DP
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

European (Non-Finnish)
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allele num: 66714
num of homozygotes: 0

Other
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num of homozygotes: 0

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

FS
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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MQ
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ClippingRankSum
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DP
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QD
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ReadPosRankSum
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SIO_000300: 7.6e-2

GenotypeDepth
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variant carriers: 0

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

Other
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allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

South Asian
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num of homozygotes: 0

East Asian
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allele frequency: 1.155535012710885e-4
allele num: 8654
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 count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele frequency: 1.199004825994425e-4
allele num: 66722
num of homozygotes: 0

Other
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num of homozygotes: 0

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

VQSLOD
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BaseQRankSum
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FS
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MQ
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MQRankSum
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ReadPosRankSum
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DP
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ClippingRankSum
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InbreedingCoeff
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QD
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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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num of homozygotes: 0

African
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allele num: 10398
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European (Non-Finnish)
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European (Finnish)
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Latino
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East Asian
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Other
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MQ
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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FS
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ClippingRankSum
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QD
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DP
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GenotypeDepth
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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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allele frequency: 1.826923076923077e-3
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East Asian
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South Asian
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European (Finnish)
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European (Non-Finnish)
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Latino
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Other
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InbreedingCoeff
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ReadPosRankSum
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FS
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ClippingRankSum
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DP
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MQRankSum
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BaseQRankSum
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VQSLOD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

African
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num of homozygotes: 0

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

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

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

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.91e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

DP
type: SiteQuality
SIO_000300: 2.831785e6

QD
type: SiteQuality
SIO_000300: 1.07e1

VQSLOD
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SIO_000300: -5.279e-1

FS
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SIO_000300: 7.945e0

InbreedingCoeff
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SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -9.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.16e-1

GenotypeDepth
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variant carriers: 3181

GenotypeDepth
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variant carriers: 472

GenotypeDepth
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variant carriers: 4199

GenotypeQuality
all individuals: 420
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variant carriers: 40

GenotypeQuality
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bin: 3.25e1
variant carriers: 3

GenotypeQuality
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bin: 4.75e1
variant carriers: 12

GenotypeQuality
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bin: 2.5e0
variant carriers: 1

GenotypeQuality
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variant carriers: 25

GenotypeQuality
all individuals: 55646
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variant carriers: 52111

GenotypeQuality
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variant carriers: 49

GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 7

GenotypeQuality
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variant carriers: 20

GenotypeQuality
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GenotypeQuality
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variant carriers: 81

GenotypeQuality
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variant carriers: 48

GenotypeQuality
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variant carriers: 14

GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 4

GenotypeQuality
all individuals: 1232
bin: 6.25e1
variant carriers: 32

Latino
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allele count: 8696
allele frequency: 7.515989628349179e-1
allele num: 11570
num of homozygotes: 3274

Other
type: Population
allele count: 605
allele frequency: 6.662995594713657e-1
allele num: 908
num of homozygotes: 195

African
type: Population
allele count: 6070
allele frequency: 5.838784147749134e-1
allele num: 10396
num of homozygotes: 1746

European (Finnish)
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allele count: 4014
allele frequency: 6.081818181818182e-1
allele num: 6600
num of homozygotes: 1227

East Asian
type: Population
allele count: 3346
allele frequency: 3.875376418809358e-1
allele num: 8634
num of homozygotes: 639

South Asian
type: Population
allele count: 8420
allele frequency: 5.099939430648092e-1
allele num: 16510
num of homozygotes: 2205

European (Non-Finnish)
type: Population
allele count: 47626
allele frequency: 7.139045449094615e-1
allele num: 66712
num of homozygotes: 17012

ClippingRankSum
type: SiteQuality
SIO_000300: -4.1e-1

MQRankSum
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SIO_000300: 1.15e-1

VQSLOD
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SIO_000300: 4.39e0

BaseQRankSum
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SIO_000300: 1.78e0

MQ
type: SiteQuality
SIO_000300: 5.957e1

FS
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SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.85e-2

ReadPosRankSum
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SIO_000300: 4.74e-1

QD
type: SiteQuality
SIO_000300: 2.487e1

DP
type: SiteQuality
SIO_000300: 5.10842e6

GenotypeDepth
all individuals: 1474
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

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

GenotypeQuality
all individuals: 1038
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variant carriers: 0

GenotypeQuality
all individuals: 49935
bin: 9.75e1
variant carriers: 2

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

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

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

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

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

DP
type: SiteQuality
SIO_000300: 4.168949e6

MQRankSum
type: SiteQuality
SIO_000300: 3.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.73e-1

MQ
type: SiteQuality
SIO_000300: 5.917e1

FS
type: SiteQuality
SIO_000300: 2.203e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.901e0

QD
type: SiteQuality
SIO_000300: 2.725e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 8.59e-1

GenotypeDepth
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variant carriers: 29

GenotypeDepth
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variant carriers: 10

GenotypeDepth
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variant carriers: 38

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 234

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

GenotypeQuality
all individuals: 1670
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variant carriers: 1

GenotypeQuality
all individuals: 1439
bin: 6.75e1
variant carriers: 0

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

Other
type: Population
allele count: 2
allele frequency: 2.207505518763797e-3
allele num: 906
num of homozygotes: 0

East Asian
type: Population
allele count: 213
allele frequency: 2.461289577074185e-2
allele num: 8654
num of homozygotes: 2

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

African
type: Population
allele count: 5
allele frequency: 4.804920238324044e-4
allele num: 10406
num of homozygotes: 0

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

South Asian
type: Population
allele count: 17
allele frequency: 1.029554263565892e-3
allele num: 16512
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.967e1

FS
type: SiteQuality
SIO_000300: 1.095e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.629999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.99e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.79e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.53e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.29e-1

DP
type: SiteQuality
SIO_000300: 4.172492e6

QD
type: SiteQuality
SIO_000300: 1.335e1

GenotypeDepth
all individuals: 9182
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
all individuals: 1897
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variant carriers: 0

GenotypeQuality
all individuals: 10
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2203
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

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

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

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
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MQRankSum
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VQSLOD
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SIO_000300: 7.64e-1

FS
type: SiteQuality
SIO_000300: 8.55e-1

InbreedingCoeff
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ReadPosRankSum
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QD
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SIO_000300: 1.165e1

DP
type: SiteQuality
SIO_000300: 4.169947e6

BaseQRankSum
type: SiteQuality
SIO_000300: -8.96e-1

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495729057395475e-5
allele num: 66730
num of homozygotes: 0

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

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

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

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

East Asian
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num of homozygotes: 0

Other
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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FS
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VQSLOD
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MQ
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DP
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QD
type: SiteQuality
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

VQSLOD
type: SiteQuality
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ReadPosRankSum
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BaseQRankSum
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DP
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InbreedingCoeff
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MQRankSum
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FS
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MQ
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ClippingRankSum
type: SiteQuality
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QD
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GenotypeDepth
all individuals: 5507
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variant carriers: 1

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
all individuals: 1681
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49960
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2117
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.496133325340207e-5
allele num: 66724
num of homozygotes: 0

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: 10406
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.4e-1

QD
type: SiteQuality
SIO_000300: 1.925e1

MQ
type: SiteQuality
SIO_000300: 5.971e1

VQSLOD
type: SiteQuality
SIO_000300: -9.500999999999999e-1

FS
type: SiteQuality
SIO_000300: 7.655e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.576e0

DP
type: SiteQuality
SIO_000300: 4.169466e6

GenotypeDepth
all individuals: 1488
bin: 9.25e1
variant carriers: 36

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

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

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

GenotypeQuality
all individuals: 1961
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 57
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1159
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variant carriers: 0

GenotypeQuality
all individuals: 39
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variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
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GenotypeQuality
all individuals: 1431
bin: 7.75e1
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GenotypeQuality
all individuals: 50244
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variant carriers: 971

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1645
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 67
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variant carriers: 0

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

GenotypeQuality
all individuals: 1522
bin: 8.25e1
variant carriers: 1

African
type: Population
allele count: 937
allele frequency: 9.007883099403961e-2
allele num: 10402
num of homozygotes: 39

Latino
type: Population
allele count: 51
allele frequency: 4.406428201140488e-3
allele num: 11574
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.207505518763797e-3
allele num: 906
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 16
allele frequency: 2.398081534772182e-4
allele num: 66720
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 3.633720930232558e-4
allele num: 16512
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.402e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.41e-1

FS
type: SiteQuality
SIO_000300: 5.22e-1

DP
type: SiteQuality
SIO_000300: 4.182881e6

MQ
type: SiteQuality
SIO_000300: 5.97e1

MQRankSum
type: SiteQuality
SIO_000300: 2.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.57e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.83e-2

GenotypeDepth
all individuals: 1478
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50126
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 49
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variant carriers: 0

GenotypeQuality
all individuals: 51
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 1360
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GenotypeQuality
all individuals: 1008
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variant carriers: 0

GenotypeQuality
all individuals: 53
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 1174
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1547
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1670
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variant carriers: 0

GenotypeQuality
all individuals: 1450
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variant carriers: 0

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

GenotypeQuality
all individuals: 2024
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498800959232614e-5
allele num: 66720
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.97e1

VQSLOD
type: SiteQuality
SIO_000300: 5.07e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.0e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.92e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.28e-1

DP
type: SiteQuality
SIO_000300: 4.178599e6

QD
type: SiteQuality
SIO_000300: 1.152e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.61e-1

GenotypeDepth
all individuals: 3968
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1008
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variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1670
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 51
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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: 50126
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 1174
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 1360
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variant carriers: 0

GenotypeQuality
all individuals: 37
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variant carriers: 0

GenotypeQuality
all individuals: 63
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variant carriers: 0

GenotypeQuality
all individuals: 1450
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variant carriers: 0

GenotypeQuality
all individuals: 2024
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 2.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.728309713100588e-4
allele num: 11572
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.103752759381898e-3
allele num: 906
num of homozygotes: 0

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

South Asian
type: Population
allele count: 3
allele frequency: 1.817080557238038e-4
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.28e-1

DP
type: SiteQuality
SIO_000300: 4.178599e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.152e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.61e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.92e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.07e0

GenotypeDepth
all individuals: 4577
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1540
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variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1170
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 1672
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variant carriers: 0

GenotypeQuality
all individuals: 2014
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variant carriers: 0

GenotypeQuality
all individuals: 1347
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1003
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 3.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49902563333833e-5
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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.6583e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.379999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.887e0

DP
type: SiteQuality
SIO_000300: 4.178528e6

QD
type: SiteQuality
SIO_000300: 1.066e1

VQSLOD
type: SiteQuality
SIO_000300: -2.409e0

MQRankSum
type: SiteQuality
SIO_000300: -6.33e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

GenotypeDepth
all individuals: 3969
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1980
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variant carriers: 0

GenotypeQuality
all individuals: 68
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1353
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
all individuals: 1010
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1173
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1454
bin: 7.75e1
variant carriers: 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: 8654
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66716
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.615384615384615e-5
allele num: 10400
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.24e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.69e0

MQRankSum
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SIO_000300: 1.98e0

DP
type: SiteQuality
SIO_000300: 4.178311e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.5e-3

FS
type: SiteQuality
SIO_000300: 3.676e0

QD
type: SiteQuality
SIO_000300: 1.586e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e0

MQ
type: SiteQuality
SIO_000300: 5.991e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.61e-1

GenotypeDepth
all individuals: 4588
bin: 6.75e1
variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 29

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66712
num of homozygotes: 0

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

East Asian
type: Population
allele count: 29
allele frequency: 3.351051536861567e-3
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 4.178937e6

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.115e0

MQRankSum
type: SiteQuality
SIO_000300: 1.67e-1

InbreedingCoeff
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SIO_000300: 4.7e-3

ReadPosRankSum
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VQSLOD
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BaseQRankSum
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SIO_000300: -1.278e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.1e-2

GenotypeDepth
all individuals: 5028
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 28
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1453
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1336
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50158
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1542
bin: 8.25e1
variant carriers: 0

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

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

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