http://identifiers.org/exac.variant/11-89182630-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89182630
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89182630
    reference: chr 11
allele count: 18
allele frequency: 1.493428912783751e-4
allele num: 120528
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.327T>G
  hgvsp: ENST00000534731.1:c.327T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-16606T>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.255T>G
  hgvsp: ENST00000542487.1:c.255T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.252T>G
  hgvsp: ENST00000528341.1:c.252T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.255T>G
  hgvsp: ENST00000532825.1:c.255T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.255T>G
  hgvsp: ENST00000424319.1:c.255T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.390T>G
  hgvsp: ENST00000413594.2:c.390T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.255T>G
  hgvsp: ENST00000535633.1:c.255T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.327T>G
  hgvsp: ENST00000263317.4:c.327T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+40996T>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.255T>G
  hgvsp: ENST00000343727.5:c.255T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.327T>G
  hgvsp: ENST00000529343.1:c.327T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+40996T>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.255T>G
  hgvsp: ENST00000527956.1:c.255T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.327T>G
  hgvsp: ENST00000525196.1:c.327T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.475T>G
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9363
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gly109Gly
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

http://identifiers.org/exac.variant/11-89182639-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89182639
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89182639
    reference: chr 11
allele count: 5
allele frequency: 4.143119935035879e-5
allele num: 120682
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.318T>G
  hgvsp: ENSP00000436716.1:p.Ile106Met
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.466T>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.318T>G
  hgvsp: ENSP00000263317.4:p.Ile106Met
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.246T>G
  hgvsp: ENSP00000434924.1:p.Ile82Met
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.246T>G
  hgvsp: ENSP00000439373.1:p.Ile82Met
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.243T>G
  hgvsp: ENSP00000436970.1:p.Ile81Met
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.318T>G
  hgvsp: ENSP00000436892.1:p.Ile106Met
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+40987T>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.246T>G
  hgvsp: ENSP00000433797.1:p.Ile82Met
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.246T>G
  hgvsp: ENSP00000440172.1:p.Ile82Met
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.318T>G
  hgvsp: ENSP00000435474.1:p.Ile106Met
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+40987T>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.246T>G
  hgvsp: ENSP00000412446.1:p.Ile82Met
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.381T>G
  hgvsp: ENSP00000405705.2:p.Ile127Met
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.246T>G
  hgvsp: ENSP00000344747.5:p.Ile82Met
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-16615T>G
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3116
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile106Met
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

11-89182642-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89182642
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89182642
    reference: chr 11
allele count: 1
allele frequency: 8.284043275842073e-6
allele num: 120714
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.463T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.243T>C
  hgvsp: ENST00000424319.1:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.315T>C
  hgvsp: ENST00000263317.4:c.315T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.378T>C
  hgvsp: ENST00000413594.2:c.378T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.243T>C
  hgvsp: ENST00000532825.1:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.240T>C
  hgvsp: ENST00000528341.1:c.240T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.243T>C
  hgvsp: ENST00000343727.5:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.243T>C
  hgvsp: ENST00000527956.1:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.243T>C
  hgvsp: ENST00000535633.1:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.315T>C
  hgvsp: ENST00000529343.1:c.315T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.243T>C
  hgvsp: ENST00000542487.1:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+40984T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+40984T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-16618T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.315T>C
  hgvsp: ENST00000525196.1:c.315T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.315T>C
  hgvsp: ENST00000534731.1:c.315T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9515
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His105His
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ

http://identifiers.org/exac.variant/11-89182646-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89182646
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89182646
    reference: chr 11
allele count: 12
allele frequency: 9.936571551595648e-5
allele num: 120766
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.236T>G
  hgvsp: ENSP00000436970.1:p.Phe79Cys
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.374T>G
  hgvsp: ENSP00000405705.2:p.Phe125Cys
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+40980T>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.311T>G
  hgvsp: ENSP00000263317.4:p.Phe104Cys
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+40980T>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.239T>G
  hgvsp: ENSP00000434924.1:p.Phe80Cys
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.239T>G
  hgvsp: ENSP00000412446.1:p.Phe80Cys
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.311T>G
  hgvsp: ENSP00000436892.1:p.Phe104Cys
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.239T>G
  hgvsp: ENSP00000433797.1:p.Phe80Cys
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.239T>G
  hgvsp: ENSP00000344747.5:p.Phe80Cys
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.239T>G
  hgvsp: ENSP00000439373.1:p.Phe80Cys
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.311T>G
  hgvsp: ENSP00000435474.1:p.Phe104Cys
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.311T>G
  hgvsp: ENSP00000436716.1:p.Phe104Cys
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.239T>G
  hgvsp: ENSP00000440172.1:p.Phe80Cys
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.459T>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-16622T>G
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9536
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3114
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe104Cys
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: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

11-89182648-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89182648
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89182648
    reference: chr 11
allele count: 1
allele frequency: 8.280064915708939e-6
allele num: 120772
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-16624A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.237A>G
  hgvsp: ENST00000532825.1:c.237A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+40978A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.372A>G
  hgvsp: ENST00000413594.2:c.372A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.309A>G
  hgvsp: ENST00000529343.1:c.309A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.237A>G
  hgvsp: ENST00000535633.1:c.237A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.309A>G
  hgvsp: ENST00000263317.4:c.309A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.237A>G
  hgvsp: ENST00000542487.1:c.237A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.457A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.237A>G
  hgvsp: ENST00000527956.1:c.237A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.234A>G
  hgvsp: ENST00000528341.1:c.234A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.237A>G
  hgvsp: ENST00000424319.1:c.237A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.309A>G
  hgvsp: ENST00000534731.1:c.309A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.309A>G
  hgvsp: ENST00000525196.1:c.309A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.237A>G
  hgvsp: ENST00000343727.5:c.237A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+40978A>G
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43232
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3115
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr103Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP

11-89182649-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89182649
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89182649
    reference: chr 11
allele count: 1
allele frequency: 8.279790686891435e-6
allele num: 120776
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.233C>T
  hgvsp: ENSP00000436970.1:p.Thr78Ile
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+40977C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.236C>T
  hgvsp: ENSP00000434924.1:p.Thr79Ile
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.308C>T
  hgvsp: ENSP00000436716.1:p.Thr103Ile
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.236C>T
  hgvsp: ENSP00000344747.5:p.Thr79Ile
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.456C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.236C>T
  hgvsp: ENSP00000439373.1:p.Thr79Ile
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.308C>T
  hgvsp: ENSP00000263317.4:p.Thr103Ile
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.236C>T
  hgvsp: ENSP00000412446.1:p.Thr79Ile
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.236C>T
  hgvsp: ENSP00000433797.1:p.Thr79Ile
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+40977C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.236C>T
  hgvsp: ENSP00000440172.1:p.Thr79Ile
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.308C>T
  hgvsp: ENSP00000436892.1:p.Thr103Ile
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-16625C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.308C>T
  hgvsp: ENSP00000435474.1:p.Thr103Ile
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.371C>T
  hgvsp: ENSP00000405705.2:p.Thr124Ile
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43236
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr103Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

11-89182652-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89182652
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89182652
    reference: chr 11
allele count: 64
allele frequency: 5.298539590025499e-4
allele num: 120788
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.305G>A
  hgvsp: ENSP00000263317.4:p.Arg102Lys
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.368G>A
  hgvsp: ENSP00000405705.2:p.Arg123Lys
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.305G>A
  hgvsp: ENSP00000435474.1:p.Arg102Lys
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.453G>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.233G>A
  hgvsp: ENSP00000434924.1:p.Arg78Lys
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.230G>A
  hgvsp: ENSP00000436970.1:p.Arg77Lys
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.305G>A
  hgvsp: ENSP00000436892.1:p.Arg102Lys
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.233G>A
  hgvsp: ENSP00000433797.1:p.Arg78Lys
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+40974G>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.233G>A
  hgvsp: ENSP00000440172.1:p.Arg78Lys
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.233G>A
  hgvsp: ENSP00000439373.1:p.Arg78Lys
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-16628G>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.233G>A
  hgvsp: ENSP00000344747.5:p.Arg78Lys
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.233G>A
  hgvsp: ENSP00000412446.1:p.Arg78Lys
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+40974G>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.305G>A
  hgvsp: ENSP00000436716.1:p.Arg102Lys
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9554
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 4.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg102Lys
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP

11-89182658-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89182658
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89182658
    reference: chr 11
allele count: 1
allele frequency: 8.277186418792524e-6
allele num: 120814
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+40968A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.299A>G
  hgvsp: ENSP00000435474.1:p.Lys100Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-16634A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.227A>G
  hgvsp: ENSP00000412446.1:p.Lys76Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.227A>G
  hgvsp: ENSP00000433797.1:p.Lys76Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.224A>G
  hgvsp: ENSP00000436970.1:p.Lys75Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+40968A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.227A>G
  hgvsp: ENSP00000344747.5:p.Lys76Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.362A>G
  hgvsp: ENSP00000405705.2:p.Lys121Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.299A>G
  hgvsp: ENSP00000263317.4:p.Lys100Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.299A>G
  hgvsp: ENSP00000436716.1:p.Lys100Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.227A>G
  hgvsp: ENSP00000440172.1:p.Lys76Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.227A>G
  hgvsp: ENSP00000434924.1:p.Lys76Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.447A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.227A>G
  hgvsp: ENSP00000439373.1:p.Lys76Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.299A>G
  hgvsp: ENSP00000436892.1:p.Lys100Arg
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9608
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys100Arg
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ClippingRankSum

11-89182663-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89182663
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89182663
    reference: chr 11
allele count: 1
allele frequency: 8.276912380605539e-6
allele num: 120818
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.222G>C
  hgvsp: ENSP00000439373.1:p.Leu74Phe
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.357G>C
  hgvsp: ENSP00000405705.2:p.Leu119Phe
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.294G>C
  hgvsp: ENSP00000263317.4:p.Leu98Phe
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.222G>C
  hgvsp: ENSP00000344747.5:p.Leu74Phe
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.219G>C
  hgvsp: ENSP00000436970.1:p.Leu73Phe
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.222G>C
  hgvsp: ENSP00000412446.1:p.Leu74Phe
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.442G>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.222G>C
  hgvsp: ENSP00000440172.1:p.Leu74Phe
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-16639G>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.222G>C
  hgvsp: ENSP00000433797.1:p.Leu74Phe
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.222G>C
  hgvsp: ENSP00000434924.1:p.Leu74Phe
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+40963G>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.294G>C
  hgvsp: ENSP00000435474.1:p.Leu98Phe
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+40963G>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.294G>C
  hgvsp: ENSP00000436892.1:p.Leu98Phe
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.294G>C
  hgvsp: ENSP00000436716.1:p.Leu98Phe
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43126
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9618
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu98Phe
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/11-89182664-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89182664
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89182664
    reference: chr 11
allele count: 2
allele frequency: 1.655327672112695e-5
allele num: 120822
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+40962T>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.221T>G
  hgvsp: ENSP00000434924.1:p.Leu74Trp
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.356T>G
  hgvsp: ENSP00000405705.2:p.Leu119Trp
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.441T>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-16640T>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.218T>G
  hgvsp: ENSP00000436970.1:p.Leu73Trp
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.221T>G
  hgvsp: ENSP00000344747.5:p.Leu74Trp
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.293T>G
  hgvsp: ENSP00000436892.1:p.Leu98Trp
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.221T>G
  hgvsp: ENSP00000433797.1:p.Leu74Trp
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.293T>G
  hgvsp: ENSP00000263317.4:p.Leu98Trp
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+40962T>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.221T>G
  hgvsp: ENSP00000439373.1:p.Leu74Trp
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.293T>G
  hgvsp: ENSP00000436716.1:p.Leu98Trp
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.221T>G
  hgvsp: ENSP00000440172.1:p.Leu74Trp
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.221T>G
  hgvsp: ENSP00000412446.1:p.Leu74Trp
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.293T>G
  hgvsp: ENSP00000435474.1:p.Leu98Trp
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu98Trp
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

11-89182665-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89182665
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89182665
    reference: chr 11
allele count: 1
allele frequency: 8.276638360563474e-6
allele num: 120822
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.292T>C
  hgvsp: ENST00000534731.1:c.292T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.220T>C
  hgvsp: ENST00000542487.1:c.220T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.292T>C
  hgvsp: ENST00000529343.1:c.292T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.292T>C
  hgvsp: ENST00000263317.4:c.292T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.220T>C
  hgvsp: ENST00000527956.1:c.220T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.292T>C
  hgvsp: ENST00000525196.1:c.292T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.220T>C
  hgvsp: ENST00000343727.5:c.220T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.355T>C
  hgvsp: ENST00000413594.2:c.355T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.217T>C
  hgvsp: ENST00000528341.1:c.217T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.220T>C
  hgvsp: ENST00000532825.1:c.220T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.220T>C
  hgvsp: ENST00000424319.1:c.220T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+40961T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.440T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+40961T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-16641T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.220T>C
  hgvsp: ENST00000535633.1:c.220T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu98Leu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum

http://identifiers.org/exac.variant/11-89182666-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89182666
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89182666
    reference: chr 11
allele count: 180
allele frequency: 1.489942885522722e-3
allele num: 120810
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.219G>T
  hgvsp: ENSP00000434924.1:p.Leu73Phe
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.219G>T
  hgvsp: ENSP00000439373.1:p.Leu73Phe
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+40960G>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.219G>T
  hgvsp: ENSP00000440172.1:p.Leu73Phe
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.219G>T
  hgvsp: ENSP00000412446.1:p.Leu73Phe
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.291G>T
  hgvsp: ENSP00000263317.4:p.Leu97Phe
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.219G>T
  hgvsp: ENSP00000344747.5:p.Leu73Phe
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.291G>T
  hgvsp: ENSP00000436716.1:p.Leu97Phe
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.354G>T
  hgvsp: ENSP00000405705.2:p.Leu118Phe
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.439G>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.291G>T
  hgvsp: ENSP00000436892.1:p.Leu97Phe
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.291G>T
  hgvsp: ENSP00000435474.1:p.Leu97Phe
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.219G>T
  hgvsp: ENSP00000433797.1:p.Leu73Phe
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.216G>T
  hgvsp: ENSP00000436970.1:p.Leu72Phe
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+40960G>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-16642G>T
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3133
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 5.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 4.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 4.75e1
  variant carriers: 18
genotype quality: GenotypeQuality
hgvs: p.Leu97Phe
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

11-89182669-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89182669
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89182669
    reference: chr 11
allele count: 1
allele frequency: 8.279653579294243e-6
allele num: 120778
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+40957A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.213A>G
  hgvsp: ENST00000528341.1:c.213A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.216A>G
  hgvsp: ENST00000424319.1:c.216A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.216A>G
  hgvsp: ENST00000542487.1:c.216A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.288A>G
  hgvsp: ENST00000529343.1:c.288A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.351A>G
  hgvsp: ENST00000413594.2:c.351A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.288A>G
  hgvsp: ENST00000263317.4:c.288A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.216A>G
  hgvsp: ENST00000343727.5:c.216A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+40957A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.216A>G
  hgvsp: ENST00000527956.1:c.216A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.216A>G
  hgvsp: ENST00000535633.1:c.216A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.288A>G
  hgvsp: ENST00000534731.1:c.288A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.216A>G
  hgvsp: ENST00000532825.1:c.216A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.436A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-16645A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.288A>G
  hgvsp: ENST00000525196.1:c.288A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9719
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg96Arg
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

11-89182672-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89182672
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89182672
    reference: chr 11
allele count: 131
allele frequency: 1.084634618887546e-3
allele num: 120778
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.213G>A
  hgvsp: ENST00000343727.5:c.213G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.285G>A
  hgvsp: ENST00000529343.1:c.285G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+40954G>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+40954G>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.210G>A
  hgvsp: ENST00000528341.1:c.210G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.213G>A
  hgvsp: ENST00000542487.1:c.213G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.213G>A
  hgvsp: ENST00000527956.1:c.213G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.213G>A
  hgvsp: ENST00000424319.1:c.213G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.213G>A
  hgvsp: ENST00000532825.1:c.213G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.348G>A
  hgvsp: ENST00000413594.2:c.348G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.285G>A
  hgvsp: ENST00000263317.4:c.285G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.213G>A
  hgvsp: ENST00000535633.1:c.213G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.285G>A
  hgvsp: ENST00000534731.1:c.285G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.433G>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.285G>A
  hgvsp: ENST00000525196.1:c.285G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-16648G>A
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 9701
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 4.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 9.75e1
  variant carriers: 22
genotype quality: GenotypeQuality
hgvs: p.Arg95Arg
num of homozygotes: 1
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum

11-89182676-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89182676
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89182676
    reference: chr 11
allele count: 2
allele frequency: 1.655903295247558e-5
allele num: 120780
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.281C>T
  hgvsp: ENSP00000263317.4:p.Thr94Ile
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.209C>T
  hgvsp: ENSP00000434924.1:p.Thr70Ile
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.209C>T
  hgvsp: ENSP00000412446.1:p.Thr70Ile
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.209C>T
  hgvsp: ENSP00000439373.1:p.Thr70Ile
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+40950C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+40950C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.281C>T
  hgvsp: ENSP00000435474.1:p.Thr94Ile
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.209C>T
  hgvsp: ENSP00000433797.1:p.Thr70Ile
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-16652C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.206C>T
  hgvsp: ENSP00000436970.1:p.Thr69Ile
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.429C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.344C>T
  hgvsp: ENSP00000405705.2:p.Thr115Ile
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.281C>T
  hgvsp: ENSP00000436716.1:p.Thr94Ile
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.209C>T
  hgvsp: ENSP00000344747.5:p.Thr70Ile
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.209C>T
  hgvsp: ENSP00000440172.1:p.Thr70Ile
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.281C>T
  hgvsp: ENSP00000436892.1:p.Thr94Ile
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3200
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr94Ile
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: DP

11-89182685-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89182685
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89182685
    reference: chr 11
allele count: 1
allele frequency: 8.285141427364165e-6
allele num: 120698
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.200G>A
  hgvsp: ENSP00000412446.1:p.Ser67Asn
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.272G>A
  hgvsp: ENSP00000435474.1:p.Ser91Asn
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.197G>A
  hgvsp: ENSP00000436970.1:p.Ser66Asn
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.200G>A
  hgvsp: ENSP00000440172.1:p.Ser67Asn
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.272G>A
  hgvsp: ENSP00000263317.4:p.Ser91Asn
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.200G>A
  hgvsp: ENSP00000344747.5:p.Ser67Asn
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.272G>A
  hgvsp: ENSP00000436892.1:p.Ser91Asn
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.200G>A
  hgvsp: ENSP00000434924.1:p.Ser67Asn
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.200G>A
  hgvsp: ENSP00000433797.1:p.Ser67Asn
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+40941G>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.335G>A
  hgvsp: ENSP00000405705.2:p.Ser112Asn
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+40941G>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.200G>A
  hgvsp: ENSP00000439373.1:p.Ser67Asn
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-16661G>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.420G>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.272G>A
  hgvsp: ENSP00000436716.1:p.Ser91Asn
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42660
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser91Asn
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

11-89182686-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89182686
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89182686
    reference: chr 11
allele count: 228
allele frequency: 1.889200072916494e-3
allele num: 120686
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.419A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+40940A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.199A>G
  hgvsp: ENSP00000433797.1:p.Ser67Gly
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.199A>G
  hgvsp: ENSP00000344747.5:p.Ser67Gly
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.199A>G
  hgvsp: ENSP00000412446.1:p.Ser67Gly
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.196A>G
  hgvsp: ENSP00000436970.1:p.Ser66Gly
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.199A>G
  hgvsp: ENSP00000439373.1:p.Ser67Gly
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.271A>G
  hgvsp: ENSP00000435474.1:p.Ser91Gly
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+40940A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.271A>G
  hgvsp: ENSP00000263317.4:p.Ser91Gly
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.199A>G
  hgvsp: ENSP00000434924.1:p.Ser67Gly
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-16662A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.271A>G
  hgvsp: ENSP00000436716.1:p.Ser91Gly
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.271A>G
  hgvsp: ENSP00000436892.1:p.Ser91Gly
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.199A>G
  hgvsp: ENSP00000440172.1:p.Ser67Gly
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.334A>G
  hgvsp: ENSP00000405705.2:p.Ser112Gly
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 5.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 9764
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 3.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 42463
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser91Gly
num of homozygotes: 1
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

11-89182688-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89182688
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89182688
    reference: chr 11
allele count: 2
allele frequency: 1.657357840131263e-5
allele num: 120674
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.197C>T
  hgvsp: ENSP00000344747.5:p.Pro66Leu
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.269C>T
  hgvsp: ENSP00000263317.4:p.Pro90Leu
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-16664C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.197C>T
  hgvsp: ENSP00000412446.1:p.Pro66Leu
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.332C>T
  hgvsp: ENSP00000405705.2:p.Pro111Leu
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+40938C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.197C>T
  hgvsp: ENSP00000434924.1:p.Pro66Leu
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.197C>T
  hgvsp: ENSP00000433797.1:p.Pro66Leu
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.197C>T
  hgvsp: ENSP00000439373.1:p.Pro66Leu
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.417C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.269C>T
  hgvsp: ENSP00000436716.1:p.Pro90Leu
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.269C>T
  hgvsp: ENSP00000436892.1:p.Pro90Leu
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.269C>T
  hgvsp: ENSP00000435474.1:p.Pro90Leu
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.197C>T
  hgvsp: ENSP00000440172.1:p.Pro66Leu
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.194C>T
  hgvsp: ENSP00000436970.1:p.Pro65Leu
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+40938C>T
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42420
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro90Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

11-89182688-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89182688
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89182688
    reference: chr 11
allele count: 2
allele frequency: 1.657357840131263e-5
allele num: 120674
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.269C>G
  hgvsp: ENSP00000263317.4:p.Pro90Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.197C>G
  hgvsp: ENSP00000433797.1:p.Pro66Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.269C>G
  hgvsp: ENSP00000435474.1:p.Pro90Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.269C>G
  hgvsp: ENSP00000436892.1:p.Pro90Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.197C>G
  hgvsp: ENSP00000440172.1:p.Pro66Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+40938C>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.197C>G
  hgvsp: ENSP00000434924.1:p.Pro66Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.197C>G
  hgvsp: ENSP00000439373.1:p.Pro66Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.197C>G
  hgvsp: ENSP00000412446.1:p.Pro66Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.332C>G
  hgvsp: ENSP00000405705.2:p.Pro111Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+40938C>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.197C>G
  hgvsp: ENSP00000344747.5:p.Pro66Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-16664C>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.194C>G
  hgvsp: ENSP00000436970.1:p.Pro65Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.417C>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.269C>G
  hgvsp: ENSP00000436716.1:p.Pro90Arg
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9839
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3242
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro90Arg
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

11-89182704-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89182704
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89182704
    reference: chr 11
allele count: 5
allele frequency: 4.151444702756559e-5
allele num: 120440
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.193-12A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.193-12A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.193-12A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.265-12A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+40922A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.265-12A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.265-12A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.413-12A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-16680A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.193-12A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.193-12A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.193-12A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.190-12A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+40922A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.328-12A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.265-12A>G
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9734
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

http://identifiers.org/exac.variant/11-89182705-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89182705
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89182705
    reference: chr 11
allele count: 4
allele frequency: 3.321486697445776e-5
allele num: 120428
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-16681G>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.265-13G>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.193-13G>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.193-13G>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.193-13G>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.193-13G>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.265-13G>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.413-13G>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+40921G>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.265-13G>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.193-13G>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.193-13G>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.190-13G>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.328-13G>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+40921G>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.265-13G>T
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9754
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3219
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

11-89182706-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89182706
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89182706
    reference: chr 11
allele count: 1
allele frequency: 8.304268393954492e-6
allele num: 120420
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+40920T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.328-14T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.193-14T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-16682T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.265-14T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.190-14T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.193-14T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.193-14T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.193-14T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.193-14T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.265-14T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.413-14T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.265-14T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+40920T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.265-14T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.193-14T>C
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3200
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

11-89182710-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89182710
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89182710
    reference: chr 11
allele count: 1
allele frequency: 8.309512730173502e-6
allele num: 120344
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.190-18T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.193-18T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-16686T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.265-18T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.193-18T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+40916T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.265-18T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.193-18T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.193-18T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.193-18T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.328-18T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.193-18T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.413-18T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.265-18T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.265-18T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+40916T>C
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40853
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/11-89182711-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89182711
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89182711
    reference: chr 11
allele count: 1
allele frequency: 8.309650828472188e-6
allele num: 120342
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.265-19T>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.265-19T>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.190-19T>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-16687T>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.193-19T>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+40915T>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.193-19T>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+40915T>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.413-19T>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.265-19T>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.265-19T>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.193-19T>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.328-19T>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.193-19T>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.193-19T>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.193-19T>G
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

11-89182711-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89182711
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89182711
    reference: chr 11
allele count: 1
allele frequency: 8.309650828472188e-6
allele num: 120342
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.193-19T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.265-19T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.265-19T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.193-19T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.265-19T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.265-19T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.193-19T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-16687T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+40915T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+40915T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.193-19T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.328-19T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.413-19T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.193-19T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.193-19T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.190-19T>C
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40865
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3186
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum

11-89182713-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89182713
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89182713
    reference: chr 11
allele count: 1
allele frequency: 8.312275568559649e-6
allele num: 120304
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.413-21T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.193-21T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.193-21T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-16689T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.190-21T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+40913T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.193-21T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.193-21T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+40913T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.265-21T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.193-21T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.193-21T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.265-21T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.265-21T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.328-21T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.265-21T>C
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3175
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9625
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: InbreedingCoeff

11-89182714-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89182714
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89182714
    reference: chr 11
allele count: 1
allele frequency: 8.312690152787244e-6
allele num: 120298
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.265-22A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.190-22A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+40912A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.265-22A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.193-22A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.193-22A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.328-22A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.193-22A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.193-22A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-16690A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.193-22A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.413-22A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.193-22A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.265-22A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+40912A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.265-22A>G
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40602
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9650
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

11-89182714-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89182714
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89182714
    reference: chr 11
allele count: 2
allele frequency: 1.662538030557449e-5
allele num: 120298
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.193-22A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-16690A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.328-22A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.265-22A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+40912A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.193-22A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.193-22A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.265-22A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.190-22A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.193-22A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.193-22A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+40912A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.193-22A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.413-22A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.265-22A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.265-22A>C
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum

11-89182723-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89182723
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89182723
    reference: chr 11
allele count: 1
allele frequency: 8.32126749546491e-6
allele num: 120174
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.193-31A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.193-31A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.265-31A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.328-31A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.193-31A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.413-31A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+40903A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.193-31A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+40903A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.193-31A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.265-31A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.193-31A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.265-31A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-16699A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.265-31A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.190-31A>C
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38688
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2210
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2208
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3132
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ

11-89182724-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89182724
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89182724
    reference: chr 11
allele count: 2
allele frequency: 1.664752201634787e-5
allele num: 120138
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.193-32T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.328-32T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.193-32T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.193-32T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.265-32T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.193-32T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.265-32T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.265-32T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.413-32T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.193-32T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.193-32T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.265-32T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+40902T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.190-32T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+40902T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-16700T>C
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37301
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3519
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2439
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

11-89182730-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89182730
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89182730
    reference: chr 11
allele count: 1
allele frequency: 8.328058896032513e-6
allele num: 120076
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.193-38T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.265-38T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.190-38T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+40896T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-16706T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.413-38T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.193-38T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.328-38T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.193-38T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.193-38T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+40896T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.265-38T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.193-38T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.193-38T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.265-38T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.265-38T>C
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36024
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2527
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3060
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8941
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP

11-89182736-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89182736
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89182736
    reference: chr 11
allele count: 1
allele frequency: 8.346548702111677e-6
allele num: 119810
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.265-44C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.193-44C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.190-44C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+40890C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.193-44C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.193-44C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.328-44C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.265-44C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.193-44C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.193-44C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.265-44C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-16712C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+40890C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.413-44C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.193-44C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.265-44C>T
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8231
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2968
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

11-89184904-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89184904
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89184904
    reference: chr 11
allele count: 3
allele frequency: 2.506223789076206e-5
allele num: 119702
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.192+49T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.412+49T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.192+49T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.327+49T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.192+49T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.189+49T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.264+49T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.192+49T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.192+49T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+38722T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.192+49T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.264+49T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.264+49T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+38722T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-18880T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.264+49T>C
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17018
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14581
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8434
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2907
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP

11-89184908-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89184908
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89184908
    reference: chr 11
allele count: 1
allele frequency: 8.34599142032082e-6
allele num: 119818
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+38718A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.264+45A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-18884A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.192+45A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.264+45A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.327+45A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.192+45A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.412+45A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.264+45A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.264+45A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.192+45A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+38718A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.192+45A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.192+45A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.189+45A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.192+45A>T
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16308
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8499
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2834
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD

11-89184912-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89184912
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89184912
    reference: chr 11
allele count: 1
allele frequency: 8.347663488989432e-6
allele num: 119794
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.264+41A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.192+41A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.264+41A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.192+41A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.192+41A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.412+41A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.192+41A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.327+41A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.192+41A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.192+41A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.264+41A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.264+41A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+38714A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+38714A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-18888A>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.189+41A>C
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2588
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3367
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17584
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8614
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17717
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

11-89184925-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89184925
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89184925
    reference: chr 11
allele count: 1
allele frequency: 8.32279113123377e-6
allele num: 120152
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.412+28T>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.192+28T>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.192+28T>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.192+28T>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.264+28T>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.189+28T>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.264+28T>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.192+28T>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+38701T>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.192+28T>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-18901T>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.264+28T>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.327+28T>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.192+28T>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+38701T>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.264+28T>A
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8947
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1711
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff

11-89184928-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89184928
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89184928
    reference: chr 11
allele count: 2
allele frequency: 1.66306336271412e-5
allele num: 120260
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.192+25A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.189+25A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.192+25A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.327+25A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.264+25A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.412+25A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.192+25A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+38698A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.264+25A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.264+25A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.192+25A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-18904A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.192+25A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.192+25A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.264+25A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+38698A>G
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18876
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8960
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: QD

11-89184936-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89184936
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89184936
    reference: chr 11
allele count: 1
allele frequency: 8.293799555452344e-6
allele num: 120572
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.192+17C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.192+17C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-18912C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.327+17C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+38690C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+38690C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.189+17C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.192+17C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.264+17C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.192+17C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.412+17C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.192+17C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.264+17C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.264+17C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.192+17C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.264+17C>T
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21225
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1721
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9075
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3393
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQ

11-89184938-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89184938
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89184938
    reference: chr 11
allele count: 6
allele frequency: 4.971743922043055e-5
allele num: 120682
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.192+15T>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.192+15T>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.264+15T>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.264+15T>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.327+15T>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.264+15T>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.412+15T>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-18914T>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.192+15T>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.192+15T>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+38688T>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+38688T>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.192+15T>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.264+15T>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.192+15T>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.189+15T>A
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3389
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1717
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19409
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

11-89184944-T-TTTTC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89184944
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89184948
    reference: chr 11
allele count: 3
allele frequency: 2.482991508169042e-5
allele num: 120822
alternate allele: TTTTC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+38678_153+38681dupGAAA
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.192+5_192+8dupGAAA
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.192+5_192+8dupGAAA
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.192+5_192+8dupGAAA
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.192+5_192+8dupGAAA
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.327+5_327+8dupGAAA
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.264+5_264+8dupGAAA
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-18924_-23-18921dupGAAA
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+38678_153+38681dupGAAA
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.264+5_264+8dupGAAA
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.192+5_192+8dupGAAA
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.192+5_192+8dupGAAA
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.189+5_189+8dupGAAA
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.264+5_264+8dupGAAA
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.264+5_264+8dupGAAA
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.412+5_412+8dupGAAA
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

11-89184946-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89184946
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89184946
    reference: chr 11
allele count: 1
allele frequency: 8.275268532463878e-6
allele num: 120842
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.264+7A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+38680A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.327+7A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.264+7A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.192+7A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.189+7A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.264+7A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.192+7A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.192+7A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.264+7A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.192+7A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.412+7A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.192+7A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.192+7A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+38680A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-18922A>T
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.264+7A>T
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

11-89184947-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89184947
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89184947
    reference: chr 11
allele count: 1
allele frequency: 8.273762245168123e-6
allele num: 120864
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.264+6A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.264+6A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.327+6A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.192+6A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-18923A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.192+6A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.192+6A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.192+6A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.192+6A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.192+6A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.412+6A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.189+6A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+38679A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.264+6A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+38679A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.264+6A>T
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.264+6A>T
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff

11-89184947-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89184947
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89184947
    reference: chr 11
allele count: 1
allele frequency: 8.273762245168123e-6
allele num: 120864
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.192+6A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.192+6A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.412+6A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.192+6A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.264+6A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.264+6A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+38679A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.192+6A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.264+6A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.192+6A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.189+6A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.192+6A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-18923A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+38679A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.264+6A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.327+6A>G
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9115
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.264+6A>G
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/11-89184948-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89184948
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89184948
    reference: chr 11
allele count: 1
allele frequency: 8.272119647938589e-6
allele num: 120888
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.192+5G>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.264+5G>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.192+5G>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.327+5G>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.264+5G>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+38678G>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.192+5G>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.264+5G>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.412+5G>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+38678G>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.192+5G>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.189+5G>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.264+5G>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.192+5G>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.192+5G>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-18924G>T
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1715
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9113
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.264+5G>T
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum

11-89184948-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89184948
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89184948
    reference: chr 11
allele count: 4
allele frequency: 3.308847859175435e-5
allele num: 120888
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.264+5G>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.412+5G>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.327+5G>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.192+5G>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.192+5G>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.264+5G>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.192+5G>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.189+5G>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.192+5G>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+38678G>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.192+5G>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.264+5G>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-18924G>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+38678G>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.192+5G>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.264+5G>C
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21402
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1715
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.264+5G>C
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff

11-89184954-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89184954
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89184954
    reference: chr 11
allele count: 1
allele frequency: 8.264872638312644e-6
allele num: 120994
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.191A>T
  hgvsp: ENSP00000434924.1:p.Lys64Met
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.263A>T
  hgvsp: ENSP00000435474.1:p.Lys88Met
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.188A>T
  hgvsp: ENSP00000436970.1:p.Lys63Met
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-18930A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.263A>T
  hgvsp: ENSP00000436892.1:p.Lys88Met
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.263A>T
  hgvsp: ENSP00000263317.4:p.Lys88Met
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.191A>T
  hgvsp: ENSP00000344747.5:p.Lys64Met
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.191A>T
  hgvsp: ENSP00000433797.1:p.Lys64Met
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.191A>T
  hgvsp: ENSP00000439373.1:p.Lys64Met
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.411A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.191A>T
  hgvsp: ENSP00000412446.1:p.Lys64Met
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.326A>T
  hgvsp: ENSP00000405705.2:p.Lys109Met
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.191A>T
  hgvsp: ENSP00000440172.1:p.Lys64Met
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+38672A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+38672A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.263A>T
  hgvsp: ENSP00000436716.1:p.Lys88Met
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Lys88Met
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff

11-89184957-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89184957
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89184957
    reference: chr 11
allele count: 3
allele frequency: 2.47843759294141e-5
allele num: 121044
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.188A>G
  hgvsp: ENSP00000439373.1:p.Gln63Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.188A>G
  hgvsp: ENSP00000412446.1:p.Gln63Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.185A>G
  hgvsp: ENSP00000436970.1:p.Gln62Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.408A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.260A>G
  hgvsp: ENSP00000263317.4:p.Gln87Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.188A>G
  hgvsp: ENSP00000434924.1:p.Gln63Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.188A>G
  hgvsp: ENSP00000344747.5:p.Gln63Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.323A>G
  hgvsp: ENSP00000405705.2:p.Gln108Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.260A>G
  hgvsp: ENSP00000436892.1:p.Gln87Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.188A>G
  hgvsp: ENSP00000433797.1:p.Gln63Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-18933A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.188A>G
  hgvsp: ENSP00000440172.1:p.Gln63Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+38669A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+38669A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.260A>G
  hgvsp: ENSP00000435474.1:p.Gln87Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.260A>G
  hgvsp: ENSP00000436716.1:p.Gln87Arg
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln87Arg
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

11-89184961-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89184961
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89184961
    reference: chr 11
allele count: 115
allele frequency: 9.496440899106509e-4
allele num: 121098
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.181T>C
  hgvsp: ENSP00000436970.1:p.Ser61Pro
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.319T>C
  hgvsp: ENSP00000405705.2:p.Ser107Pro
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-18937T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.184T>C
  hgvsp: ENSP00000439373.1:p.Ser62Pro
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.184T>C
  hgvsp: ENSP00000440172.1:p.Ser62Pro
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.184T>C
  hgvsp: ENSP00000412446.1:p.Ser62Pro
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.184T>C
  hgvsp: ENSP00000433797.1:p.Ser62Pro
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.256T>C
  hgvsp: ENSP00000436716.1:p.Ser86Pro
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.404T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.256T>C
  hgvsp: ENSP00000436892.1:p.Ser86Pro
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.184T>C
  hgvsp: ENSP00000344747.5:p.Ser62Pro
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.256T>C
  hgvsp: ENSP00000435474.1:p.Ser86Pro
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+38665T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.256T>C
  hgvsp: ENSP00000263317.4:p.Ser86Pro
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+38665T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.184T>C
  hgvsp: ENSP00000434924.1:p.Ser62Pro
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 21425
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3386
  bin: 3.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
hgvs: p.Ser86Pro
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP

11-89184961-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89184961
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89184961
    reference: chr 11
allele count: 1
allele frequency: 8.257774694875225e-6
allele num: 121098
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.184T>A
  hgvsp: ENSP00000434924.1:p.Ser62Thr
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.184T>A
  hgvsp: ENSP00000412446.1:p.Ser62Thr
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.184T>A
  hgvsp: ENSP00000440172.1:p.Ser62Thr
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.256T>A
  hgvsp: ENSP00000435474.1:p.Ser86Thr
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.404T>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+38665T>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.184T>A
  hgvsp: ENSP00000344747.5:p.Ser62Thr
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.256T>A
  hgvsp: ENSP00000436892.1:p.Ser86Thr
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.184T>A
  hgvsp: ENSP00000439373.1:p.Ser62Thr
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.181T>A
  hgvsp: ENSP00000436970.1:p.Ser61Thr
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.256T>A
  hgvsp: ENSP00000263317.4:p.Ser86Thr
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.319T>A
  hgvsp: ENSP00000405705.2:p.Ser107Thr
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.184T>A
  hgvsp: ENSP00000433797.1:p.Ser62Thr
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.256T>A
  hgvsp: ENSP00000436716.1:p.Ser86Thr
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+38665T>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-18937T>A
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3386
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser86Thr
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP

11-89184962-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89184962
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89184962
    reference: chr 11
allele count: 1
allele frequency: 8.257911078813503e-6
allele num: 121096
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.183A>G
  hgvsp: ENST00000424319.1:c.183A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.183A>G
  hgvsp: ENST00000532825.1:c.183A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.255A>G
  hgvsp: ENST00000534731.1:c.255A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-18938A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.255A>G
  hgvsp: ENST00000525196.1:c.255A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.255A>G
  hgvsp: ENST00000263317.4:c.255A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.180A>G
  hgvsp: ENST00000528341.1:c.180A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.183A>G
  hgvsp: ENST00000527956.1:c.183A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+38664A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.183A>G
  hgvsp: ENST00000542487.1:c.183A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+38664A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.183A>G
  hgvsp: ENST00000535633.1:c.183A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.255A>G
  hgvsp: ENST00000529343.1:c.255A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.403A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.318A>G
  hgvsp: ENST00000413594.2:c.318A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.183A>G
  hgvsp: ENST00000343727.5:c.183A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1716
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly85Gly
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP

11-89184967-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89184967
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89184967
    reference: chr 11
allele count: 1
allele frequency: 8.254639107178234e-6
allele num: 121144
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.313C>T
  hgvsp: ENSP00000405705.2:p.Arg105Ter
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.398C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.175C>T
  hgvsp: ENSP00000436970.1:p.Arg59Ter
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-18943C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.178C>T
  hgvsp: ENSP00000344747.5:p.Arg60Ter
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.178C>T
  hgvsp: ENSP00000439373.1:p.Arg60Ter
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.178C>T
  hgvsp: ENSP00000433797.1:p.Arg60Ter
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.178C>T
  hgvsp: ENSP00000434924.1:p.Arg60Ter
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.178C>T
  hgvsp: ENSP00000412446.1:p.Arg60Ter
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.250C>T
  hgvsp: ENSP00000435474.1:p.Arg84Ter
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+38659C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.250C>T
  hgvsp: ENSP00000436892.1:p.Arg84Ter
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.250C>T
  hgvsp: ENSP00000263317.4:p.Arg84Ter
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.250C>T
  hgvsp: ENSP00000436716.1:p.Arg84Ter
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.178C>T
  hgvsp: ENSP00000440172.1:p.Arg60Ter
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+38659C>T
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1717
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21431
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg84Ter
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum

11-89184975-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89184975
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89184975
    reference: chr 11
allele count: 1
allele frequency: 8.252595441266279e-6
allele num: 121174
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.170C>T
  hgvsp: ENSP00000439373.1:p.Ala57Val
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.242C>T
  hgvsp: ENSP00000436716.1:p.Ala81Val
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.170C>T
  hgvsp: ENSP00000344747.5:p.Ala57Val
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.242C>T
  hgvsp: ENSP00000263317.4:p.Ala81Val
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-18951C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.170C>T
  hgvsp: ENSP00000433797.1:p.Ala57Val
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.170C>T
  hgvsp: ENSP00000440172.1:p.Ala57Val
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.170C>T
  hgvsp: ENSP00000434924.1:p.Ala57Val
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.170C>T
  hgvsp: ENSP00000412446.1:p.Ala57Val
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.305C>T
  hgvsp: ENSP00000405705.2:p.Ala102Val
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.167C>T
  hgvsp: ENSP00000436970.1:p.Ala56Val
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.242C>T
  hgvsp: ENSP00000436892.1:p.Ala81Val
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+38651C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+38651C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.390C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.242C>T
  hgvsp: ENSP00000435474.1:p.Ala81Val
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21444
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1716
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala81Val
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

11-89184975-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89184975
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89184975
    reference: chr 11
allele count: 1
allele frequency: 8.252595441266279e-6
allele num: 121174
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.170C>G
  hgvsp: ENSP00000412446.1:p.Ala57Gly
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+38651C>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.170C>G
  hgvsp: ENSP00000439373.1:p.Ala57Gly
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.305C>G
  hgvsp: ENSP00000405705.2:p.Ala102Gly
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.170C>G
  hgvsp: ENSP00000344747.5:p.Ala57Gly
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.167C>G
  hgvsp: ENSP00000436970.1:p.Ala56Gly
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.242C>G
  hgvsp: ENSP00000435474.1:p.Ala81Gly
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.170C>G
  hgvsp: ENSP00000434924.1:p.Ala57Gly
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+38651C>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-18951C>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.390C>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.170C>G
  hgvsp: ENSP00000433797.1:p.Ala57Gly
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.170C>G
  hgvsp: ENSP00000440172.1:p.Ala57Gly
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.242C>G
  hgvsp: ENSP00000436892.1:p.Ala81Gly
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.242C>G
  hgvsp: ENSP00000263317.4:p.Ala81Gly
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.242C>G
  hgvsp: ENSP00000436716.1:p.Ala81Gly
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1716
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9130
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala81Gly
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

11-89184976-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89184976
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89184976
    reference: chr 11
allele count: 3
allele frequency: 2.475615190374808e-5
allele num: 121182
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.169G>A
  hgvsp: ENSP00000440172.1:p.Ala57Thr
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.169G>A
  hgvsp: ENSP00000434924.1:p.Ala57Thr
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.241G>A
  hgvsp: ENSP00000263317.4:p.Ala81Thr
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.241G>A
  hgvsp: ENSP00000436892.1:p.Ala81Thr
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.169G>A
  hgvsp: ENSP00000433797.1:p.Ala57Thr
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+38650G>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.241G>A
  hgvsp: ENSP00000435474.1:p.Ala81Thr
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.304G>A
  hgvsp: ENSP00000405705.2:p.Ala102Thr
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-18952G>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+38650G>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.169G>A
  hgvsp: ENSP00000439373.1:p.Ala57Thr
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.169G>A
  hgvsp: ENSP00000412446.1:p.Ala57Thr
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.389G>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.169G>A
  hgvsp: ENSP00000344747.5:p.Ala57Thr
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.166G>A
  hgvsp: ENSP00000436970.1:p.Ala56Thr
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.241G>A
  hgvsp: ENSP00000436716.1:p.Ala81Thr
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1718
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19751
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala81Thr
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/11-89184979-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89184979
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89184979
    reference: chr 11
allele count: 1
allele frequency: 8.250688932525866e-6
allele num: 121202
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.386T>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.166T>G
  hgvsp: ENSP00000344747.5:p.Leu56Val
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.166T>G
  hgvsp: ENSP00000440172.1:p.Leu56Val
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.166T>G
  hgvsp: ENSP00000433797.1:p.Leu56Val
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.166T>G
  hgvsp: ENSP00000439373.1:p.Leu56Val
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.166T>G
  hgvsp: ENSP00000412446.1:p.Leu56Val
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.238T>G
  hgvsp: ENSP00000435474.1:p.Leu80Val
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.166T>G
  hgvsp: ENSP00000434924.1:p.Leu56Val
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+38647T>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.163T>G
  hgvsp: ENSP00000436970.1:p.Leu55Val
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.238T>G
  hgvsp: ENSP00000263317.4:p.Leu80Val
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-18955T>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+38647T>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.238T>G
  hgvsp: ENSP00000436716.1:p.Leu80Val
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.301T>G
  hgvsp: ENSP00000405705.2:p.Leu101Val
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.238T>G
  hgvsp: ENSP00000436892.1:p.Leu80Val
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21449
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu80Val
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

11-89184985-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89184985
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89184985
    reference: chr 11
allele count: 3
allele frequency: 2.474920802534319e-5
allele num: 121216
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.380A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.160A>G
  hgvsp: ENSP00000439373.1:p.Thr54Ala
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.160A>G
  hgvsp: ENSP00000344747.5:p.Thr54Ala
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+38641A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.157A>G
  hgvsp: ENSP00000436970.1:p.Thr53Ala
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.232A>G
  hgvsp: ENSP00000435474.1:p.Thr78Ala
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.232A>G
  hgvsp: ENSP00000436892.1:p.Thr78Ala
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.160A>G
  hgvsp: ENSP00000433797.1:p.Thr54Ala
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.160A>G
  hgvsp: ENSP00000412446.1:p.Thr54Ala
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.160A>G
  hgvsp: ENSP00000440172.1:p.Thr54Ala
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+38641A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.160A>G
  hgvsp: ENSP00000434924.1:p.Thr54Ala
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-18961A>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.232A>G
  hgvsp: ENSP00000263317.4:p.Thr78Ala
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.295A>G
  hgvsp: ENSP00000405705.2:p.Thr99Ala
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.232A>G
  hgvsp: ENSP00000436716.1:p.Thr78Ala
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19763
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1717
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr78Ala
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/11-89184987-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89184987
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89184987
    reference: chr 11
allele count: 1
allele frequency: 8.249463784853985e-6
allele num: 121220
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+38639G>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.378G>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.230G>T
  hgvsp: ENSP00000263317.4:p.Arg77Leu
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.293G>T
  hgvsp: ENSP00000405705.2:p.Arg98Leu
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.158G>T
  hgvsp: ENSP00000440172.1:p.Arg53Leu
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.158G>T
  hgvsp: ENSP00000439373.1:p.Arg53Leu
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+38639G>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.155G>T
  hgvsp: ENSP00000436970.1:p.Arg52Leu
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.230G>T
  hgvsp: ENSP00000436716.1:p.Arg77Leu
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.158G>T
  hgvsp: ENSP00000433797.1:p.Arg53Leu
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.158G>T
  hgvsp: ENSP00000412446.1:p.Arg53Leu
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.158G>T
  hgvsp: ENSP00000434924.1:p.Arg53Leu
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-18963G>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.158G>T
  hgvsp: ENSP00000344747.5:p.Arg53Leu
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.230G>T
  hgvsp: ENSP00000436892.1:p.Arg77Leu
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.230G>T
  hgvsp: ENSP00000435474.1:p.Arg77Leu
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19769
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21442
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1717
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg77Leu
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD

11-89184987-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89184987
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89184987
    reference: chr 11
allele count: 1
allele frequency: 8.249463784853985e-6
allele num: 121220
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.158G>A
  hgvsp: ENSP00000434924.1:p.Arg53Gln
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.230G>A
  hgvsp: ENSP00000263317.4:p.Arg77Gln
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.158G>A
  hgvsp: ENSP00000433797.1:p.Arg53Gln
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.158G>A
  hgvsp: ENSP00000412446.1:p.Arg53Gln
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.158G>A
  hgvsp: ENSP00000440172.1:p.Arg53Gln
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.155G>A
  hgvsp: ENSP00000436970.1:p.Arg52Gln
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.158G>A
  hgvsp: ENSP00000439373.1:p.Arg53Gln
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.230G>A
  hgvsp: ENSP00000436892.1:p.Arg77Gln
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.293G>A
  hgvsp: ENSP00000405705.2:p.Arg98Gln
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.230G>A
  hgvsp: ENSP00000435474.1:p.Arg77Gln
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.158G>A
  hgvsp: ENSP00000344747.5:p.Arg53Gln
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+38639G>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.230G>A
  hgvsp: ENSP00000436716.1:p.Arg77Gln
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+38639G>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-18963G>A
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.378G>A
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9133
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21442
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1717
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg77Gln
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/11-89184991-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89184991
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89184991
    reference: chr 11
allele count: 1
allele frequency: 8.248647221855616e-6
allele num: 121232
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-18967T>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.154T>G
  hgvsp: ENSP00000344747.5:p.Cys52Gly
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.226T>G
  hgvsp: ENSP00000435474.1:p.Cys76Gly
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.154T>G
  hgvsp: ENSP00000412446.1:p.Cys52Gly
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.154T>G
  hgvsp: ENSP00000433797.1:p.Cys52Gly
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.226T>G
  hgvsp: ENSP00000263317.4:p.Cys76Gly
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.154T>G
  hgvsp: ENSP00000439373.1:p.Cys52Gly
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.289T>G
  hgvsp: ENSP00000405705.2:p.Cys97Gly
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.151T>G
  hgvsp: ENSP00000436970.1:p.Cys51Gly
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.226T>G
  hgvsp: ENSP00000436716.1:p.Cys76Gly
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+38635T>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.154T>G
  hgvsp: ENSP00000440172.1:p.Cys52Gly
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.226T>G
  hgvsp: ENSP00000436892.1:p.Cys76Gly
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.374T>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.154T>G
  hgvsp: ENSP00000434924.1:p.Cys52Gly
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+38635T>G
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19779
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21440
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys76Gly
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum

11-89184993-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89184993
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89184993
    reference: chr 11
allele count: 14
allele frequency: 1.154810611059786e-4
allele num: 121232
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.287T>C
  hgvsp: ENSP00000405705.2:p.Met96Thr
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.149T>C
  hgvsp: ENSP00000436970.1:p.Met50Thr
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.152T>C
  hgvsp: ENSP00000440172.1:p.Met51Thr
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.152T>C
  hgvsp: ENSP00000433797.1:p.Met51Thr
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.224T>C
  hgvsp: ENSP00000436892.1:p.Met75Thr
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.372T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.224T>C
  hgvsp: ENSP00000263317.4:p.Met75Thr
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+38633T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.224T>C
  hgvsp: ENSP00000435474.1:p.Met75Thr
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.152T>C
  hgvsp: ENSP00000434924.1:p.Met51Thr
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.152T>C
  hgvsp: ENSP00000412446.1:p.Met51Thr
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.152T>C
  hgvsp: ENSP00000439373.1:p.Met51Thr
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-18969T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+38633T>C
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.152T>C
  hgvsp: ENSP00000344747.5:p.Met51Thr
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.224T>C
  hgvsp: ENSP00000436716.1:p.Met75Thr
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met75Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD

11-89184996-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89184996
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89184996
    reference: chr 11
allele count: 1
allele frequency: 8.248511143738554e-6
allele num: 121234
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+38630C>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.221C>G
  hgvsp: ENSP00000435474.1:p.Pro74Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.149C>G
  hgvsp: ENSP00000434924.1:p.Pro50Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.369C>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+38630C>G
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.221C>G
  hgvsp: ENSP00000436892.1:p.Pro74Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.149C>G
  hgvsp: ENSP00000433797.1:p.Pro50Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.221C>G
  hgvsp: ENSP00000436716.1:p.Pro74Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.146C>G
  hgvsp: ENSP00000436970.1:p.Pro49Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.221C>G
  hgvsp: ENSP00000263317.4:p.Pro74Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.149C>G
  hgvsp: ENSP00000440172.1:p.Pro50Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.149C>G
  hgvsp: ENSP00000412446.1:p.Pro50Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.149C>G
  hgvsp: ENSP00000344747.5:p.Pro50Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.284C>G
  hgvsp: ENSP00000405705.2:p.Pro95Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.149C>G
  hgvsp: ENSP00000439373.1:p.Pro50Arg
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-18972C>G
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21430
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro74Arg
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

11-89184997-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89184997
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89184997
    reference: chr 11
allele count: 2
allele frequency: 1.649756660892518e-5
allele num: 121230
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.148C>T
  hgvsp: ENSP00000434924.1:p.Pro50Ser
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-18973C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.148C>T
  hgvsp: ENSP00000412446.1:p.Pro50Ser
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.220C>T
  hgvsp: ENSP00000436716.1:p.Pro74Ser
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.368C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+38629C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.148C>T
  hgvsp: ENSP00000344747.5:p.Pro50Ser
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.145C>T
  hgvsp: ENSP00000436970.1:p.Pro49Ser
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.220C>T
  hgvsp: ENSP00000263317.4:p.Pro74Ser
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.148C>T
  hgvsp: ENSP00000439373.1:p.Pro50Ser
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.148C>T
  hgvsp: ENSP00000433797.1:p.Pro50Ser
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.148C>T
  hgvsp: ENSP00000440172.1:p.Pro50Ser
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.283C>T
  hgvsp: ENSP00000405705.2:p.Pro95Ser
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+38629C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.220C>T
  hgvsp: ENSP00000436892.1:p.Pro74Ser
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.220C>T
  hgvsp: ENSP00000435474.1:p.Pro74Ser
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19789
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro74Ser
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

11-89185009-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89185009
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89185009
    reference: chr 11
allele count: 1
allele frequency: 8.249191579225235e-6
allele num: 121224
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+38617C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.133C>T
  hgvsp: ENSP00000436970.1:p.Leu45Phe
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.136C>T
  hgvsp: ENSP00000439373.1:p.Leu46Phe
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.208C>T
  hgvsp: ENSP00000436892.1:p.Leu70Phe
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.208C>T
  hgvsp: ENSP00000435474.1:p.Leu70Phe
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.136C>T
  hgvsp: ENSP00000433797.1:p.Leu46Phe
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-18985C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.136C>T
  hgvsp: ENSP00000344747.5:p.Leu46Phe
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.136C>T
  hgvsp: ENSP00000412446.1:p.Leu46Phe
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.271C>T
  hgvsp: ENSP00000405705.2:p.Leu91Phe
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.208C>T
  hgvsp: ENSP00000436716.1:p.Leu70Phe
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.136C>T
  hgvsp: ENSP00000440172.1:p.Leu46Phe
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.356C>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.208C>T
  hgvsp: ENSP00000263317.4:p.Leu70Phe
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.136C>T
  hgvsp: ENSP00000434924.1:p.Leu46Phe
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+38617C>T
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9140
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu70Phe
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum

11-89185012-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89185012
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 89185012
    reference: chr 11
allele count: 1
allele frequency: 8.248919391559706e-6
allele num: 121228
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436892
  ensembl transcript: ENST00000534731
  gene symbol: NOX4
  hgvsc: ENST00000534731.1:c.205A>T
  hgvsp: ENSP00000436892.1:p.Ser69Cys
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000440172
  ensembl transcript: ENST00000535633
  gene symbol: NOX4
  hgvsc: ENST00000535633.1:c.133A>T
  hgvsp: ENSP00000440172.1:p.Ser45Cys
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436970
  ensembl transcript: ENST00000528341
  gene symbol: NOX4
  hgvsc: ENST00000528341.1:c.130A>T
  hgvsp: ENSP00000436970.1:p.Ser44Cys
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436093
  ensembl transcript: ENST00000527626
  gene symbol: NOX4
  hgvsc: ENST00000527626.1:c.-23-18988A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000433797
  ensembl transcript: ENST00000527956
  gene symbol: NOX4
  hgvsc: ENST00000527956.1:c.133A>T
  hgvsp: ENSP00000433797.1:p.Ser45Cys
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435474
  ensembl transcript: ENST00000529343
  gene symbol: NOX4
  hgvsc: ENST00000529343.1:c.205A>T
  hgvsp: ENSP00000435474.1:p.Ser69Cys
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086991
  ensembl transcript: ENST00000525278
  gene symbol: NOX4
  hgvsc: ENST00000525278.1:n.353A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000434924
  ensembl transcript: ENST00000532825
  gene symbol: NOX4
  hgvsc: ENST00000532825.1:c.133A>T
  hgvsp: ENSP00000434924.1:p.Ser45Cys
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000412446
  ensembl transcript: ENST00000424319
  gene symbol: NOX4
  hgvsc: ENST00000424319.1:c.133A>T
  hgvsp: ENSP00000412446.1:p.Ser45Cys
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000439373
  ensembl transcript: ENST00000542487
  gene symbol: NOX4
  hgvsc: ENST00000542487.1:c.133A>T
  hgvsp: ENSP00000439373.1:p.Ser45Cys
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000263317
  ensembl transcript: ENST00000263317
  gene symbol: NOX4
  hgvsc: ENST00000263317.4:c.205A>T
  hgvsp: ENSP00000263317.4:p.Ser69Cys
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000436716
  ensembl transcript: ENST00000525196
  gene symbol: NOX4
  hgvsc: ENST00000525196.1:c.205A>T
  hgvsp: ENSP00000436716.1:p.Ser69Cys
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000435039
  ensembl transcript: ENST00000531342
  gene symbol: NOX4
  hgvsc: ENST00000531342.1:c.153+38614A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000344747
  ensembl transcript: ENST00000343727
  gene symbol: NOX4
  hgvsc: ENST00000343727.5:c.133A>T
  hgvsp: ENSP00000344747.5:p.Ser45Cys
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000365146
  ensembl transcript: ENST00000375979
  gene symbol: NOX4
  hgvsc: ENST00000375979.3:c.153+38614A>T
  variant of: http://identifiers.org/hgnc/7891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086991
  ensembl protein: ENSP00000405705
  ensembl transcript: ENST00000413594
  gene symbol: NOX4
  hgvsc: ENST00000413594.2:c.268A>T
  hgvsp: ENSP00000405705.2:p.Ser90Cys
  variant of: http://identifiers.org/hgnc/7891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ser69Cys
num of homozygotes: 0
reference allele: T

GenotypeDepth
all individuals: 3100
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 48
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 43273
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 104
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 62
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 360
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 219
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 537
bin: 9.75e1
variant carriers: 4

GenotypeDepth
all individuals: 86
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 931
bin: 3.75e1
variant carriers: 3

GenotypeDepth
all individuals: 245
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 119
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 178
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 39
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1656
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 59
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1836
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5554
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44847
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3878
bin: 9.75e1
variant carriers: 18

GenotypeQuality
all individuals: 600
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1170
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11374
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 18
allele frequency: 2.715259759850359e-4
allele num: 66292
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16446
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.8e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.7e-1

FS
type: SiteQuality
SIO_000300: 1.993e0

DP
type: SiteQuality
SIO_000300: 1.558644e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.43e0

MQRankSum
type: SiteQuality
SIO_000300: 4.8e-2

QD
type: SiteQuality
SIO_000300: 1.264e1

GenotypeDepth
all individuals: 43243
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 290
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 35
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 219
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 118
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 338
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 534
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 79
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 87
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 180
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9492
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 144
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 392
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1175
bin: 8.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 473
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44968
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1839
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 603
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5589
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1656
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3871
bin: 9.75e1
variant carriers: 5

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66382
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11394
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.036560184622859e-4
allele num: 16466
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 9.340000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.3e-1

DP
type: SiteQuality
SIO_000300: 1.560756e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.99e-1

FS
type: SiteQuality
SIO_000300: 6.384e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.47e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.77e0

QD
type: SiteQuality
SIO_000300: 1.291e1

GenotypeDepth
all individuals: 43242
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 474
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 392
bin: 5.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 79
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 98
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3116
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 338
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 620
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 143
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 180
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 118
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1838
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 473
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44994
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1175
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 603
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3869
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5593
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1656
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.775008775008775e-5
allele num: 11396
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66396
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16470
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 5.5e0

DP
type: SiteQuality
SIO_000300: 1.561036e6

MQRankSum
type: SiteQuality
SIO_000300: 9.55e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.926e-1

QD
type: SiteQuality
SIO_000300: 1.088e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.3e-1

FS
type: SiteQuality
SIO_000300: 7.931e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.81e-1

MQ
type: SiteQuality
SIO_000300: 5.919e1

GenotypeDepth
all individuals: 121
bin: 8.25e1
variant carriers: 3

GenotypeDepth
all individuals: 932
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 72
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 534
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 43242
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 245
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 250
bin: 7.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 476
bin: 4.75e1
variant carriers: 2

GenotypeDepth
all individuals: 144
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 87
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 99
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 181
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 27
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 473
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3879
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1175
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 603
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 45019
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1655
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5595
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1838
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 12
allele frequency: 1.396648044692737e-3
allele num: 8592
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11404
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66416
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

DP
type: SiteQuality
SIO_000300: 1.562131e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.26e0

MQRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

MQ
type: SiteQuality
SIO_000300: 5.956e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.69e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e0

QD
type: SiteQuality
SIO_000300: 1.197e1

GenotypeDepth
all individuals: 393
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 475
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 118
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 933
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 143
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 244
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 72
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 98
bin: 8.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 87
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 622
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 180
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 534
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45002
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 604
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1655
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3872
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 5600
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1839
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1175
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 473
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505525277769414e-5
allele num: 66422
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11404
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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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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QD
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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MQ
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BaseQRankSum
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VQSLOD
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FS
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ClippingRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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African
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Other
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East Asian
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MQ
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DP
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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FS
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VQSLOD
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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African
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Other
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South Asian
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ClippingRankSum
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QD
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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MQ
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VQSLOD
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FS
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InbreedingCoeff
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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South Asian
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European (Non-Finnish)
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Latino
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East Asian
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FS
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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DP
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VQSLOD
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MQ
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QD
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ClippingRankSum
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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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African
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South Asian
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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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ClippingRankSum
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FS
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MQ
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QD
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DP
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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European (Non-Finnish)
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East Asian
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African
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European (Finnish)
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Latino
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DP
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FS
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MQRankSum
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QD
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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MQ
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ClippingRankSum
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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
all individuals: 605
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GenotypeQuality
all individuals: 1838
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66440
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.756567425569177e-5
allele num: 11420
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

FS
type: SiteQuality
SIO_000300: 5.458e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.079e1

VQSLOD
type: SiteQuality
SIO_000300: 4.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.12e0

DP
type: SiteQuality
SIO_000300: 1.56326e6

MQRankSum
type: SiteQuality
SIO_000300: 1.16e0

GenotypeDepth
all individuals: 359
bin: 5.75e1
variant carriers: 21

GenotypeDepth
all individuals: 958
bin: 3.75e1
variant carriers: 16

GenotypeDepth
all individuals: 236
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variant carriers: 16

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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variant carriers: 3

GenotypeDepth
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 19

GenotypeDepth
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variant carriers: 15

GenotypeDepth
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variant carriers: 5

GenotypeDepth
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variant carriers: 2

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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 179

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1828
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variant carriers: 0

GenotypeQuality
all individuals: 601
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 4
allele frequency: 3.850596842510589e-4
allele num: 10388
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

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

Latino
type: Population
allele count: 9
allele frequency: 7.880910683012259e-4
allele num: 11420
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 143
allele frequency: 2.152577071290944e-3
allele num: 66432
num of homozygotes: 0

South Asian
type: Population
allele count: 24
allele frequency: 1.455780662380201e-3
allele num: 16486
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.570141e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

MQ
type: SiteQuality
SIO_000300: 5.975e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: -1.787e0

VQSLOD
type: SiteQuality
SIO_000300: 4.68e0

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.22e-1

QD
type: SiteQuality
SIO_000300: 9.960000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-2

GenotypeDepth
all individuals: 237
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 340
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 221
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variant carriers: 0

GenotypeDepth
all individuals: 952
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variant carriers: 0

GenotypeDepth
all individuals: 395
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 42913
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variant carriers: 0

GenotypeDepth
all individuals: 3170
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 180
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variant carriers: 0

GenotypeDepth
all individuals: 145
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variant carriers: 0

GenotypeQuality
all individuals: 87
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GenotypeQuality
all individuals: 1839
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variant carriers: 0

GenotypeQuality
all individuals: 20
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GenotypeQuality
all individuals: 603
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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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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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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
all individuals: 1176
bin: 8.25e1
variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11418
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66412
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.066488716330988e-5
allele num: 16484
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.634e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

FS
type: SiteQuality
SIO_000300: 1.177e0

QD
type: SiteQuality
SIO_000300: 1.001e1

MQ
type: SiteQuality
SIO_000300: 5.88e1

MQRankSum
type: SiteQuality
SIO_000300: 1.65e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.49e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.33e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.87e-1

DP
type: SiteQuality
SIO_000300: 1.563953e6

GenotypeDepth
all individuals: 42835
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 190
bin: 7.25e1
variant carriers: 12

GenotypeDepth
all individuals: 228
bin: 6.75e1
variant carriers: 8

GenotypeDepth
all individuals: 236
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variant carriers: 0

GenotypeDepth
all individuals: 492
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variant carriers: 13

GenotypeDepth
all individuals: 65
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GenotypeDepth
all individuals: 119
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variant carriers: 3

GenotypeDepth
all individuals: 99
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GenotypeDepth
all individuals: 3168
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variant carriers: 6

GenotypeDepth
all individuals: 88
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variant carriers: 1

GenotypeDepth
all individuals: 350
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variant carriers: 12

GenotypeDepth
all individuals: 254
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variant carriers: 8

GenotypeDepth
all individuals: 155
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variant carriers: 10

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 1655
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GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 35
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GenotypeQuality
all individuals: 63
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GenotypeQuality
all individuals: 70
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GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 24
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GenotypeQuality
all individuals: 1834
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 34
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GenotypeQuality
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GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 475
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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: 128

GenotypeQuality
all individuals: 1171
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 92
allele frequency: 1.385291814732277e-3
allele num: 66412
num of homozygotes: 1

African
type: Population
allele count: 6
allele frequency: 5.780346820809249e-4
allele num: 10380
num of homozygotes: 0

Latino
type: Population
allele count: 13
allele frequency: 1.13875262789068e-3
allele num: 11416
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.518372304889159e-4
allele num: 6586
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

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

South Asian
type: Population
allele count: 19
allele frequency: 1.152632856102888e-3
allele num: 16484
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.977e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.09e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.08e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.64e-1

QD
type: SiteQuality
SIO_000300: 1.153e1

FS
type: SiteQuality
SIO_000300: 5.26e-1

DP
type: SiteQuality
SIO_000300: 1.56932e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.541e0

MQRankSum
type: SiteQuality
SIO_000300: 2.71e-1

GenotypeDepth
all individuals: 63
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3889
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variant carriers: 2

GenotypeQuality
all individuals: 1660
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GenotypeQuality
all individuals: 40
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GenotypeQuality
all individuals: 28
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 5605
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 68
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variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11418
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66412
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.327746741154562e-4
allele num: 8592
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 7.41e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

BaseQRankSum
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SIO_000300: -1.813e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

QD
type: SiteQuality
SIO_000300: 1.265e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.6e-2

FS
type: SiteQuality
SIO_000300: 3.233e0

DP
type: SiteQuality
SIO_000300: 1.56486e6

GenotypeDepth
all individuals: 9768
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 60
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GenotypeQuality
all individuals: 1179
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506931886678722e-5
allele num: 66360
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11414
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

FS
type: SiteQuality
SIO_000300: 1.068e0

MQ
type: SiteQuality
SIO_000300: 5.947e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.41e0

VQSLOD
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SIO_000300: -3.159e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.31e0

QD
type: SiteQuality
SIO_000300: 2.953e1

DP
type: SiteQuality
SIO_000300: 1.563699e6

MQRankSum
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SIO_000300: 2.08e0

ClippingRankSum
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SIO_000300: 2.14e0

GenotypeDepth
all individuals: 559
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variant carriers: 25

GenotypeDepth
all individuals: 271
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variant carriers: 0

GenotypeDepth
all individuals: 649
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variant carriers: 15

GenotypeDepth
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variant carriers: 11

GenotypeDepth
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GenotypeDepth
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variant carriers: 17

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 6

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
all individuals: 35
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variant carriers: 0

African
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allele count: 8
allele frequency: 7.714561234329798e-4
allele num: 10370
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

European (Finnish)
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allele count: 5
allele frequency: 7.596475235490732e-4
allele num: 6582
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 196
allele frequency: 2.953586497890295e-3
allele num: 66360
num of homozygotes: 1

South Asian
type: Population
allele count: 10
allele frequency: 6.072382803011902e-4
allele num: 16468
num of homozygotes: 0

Latino
type: Population
allele count: 8
allele frequency: 7.008936393902226e-4
allele num: 11414
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.978e1

VQSLOD
type: SiteQuality
SIO_000300: 5.45e0

ClippingRankSum
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SIO_000300: -8.2e-2

ReadPosRankSum
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SIO_000300: 5.78e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.16e-1

QD
type: SiteQuality
SIO_000300: 1.351e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.2e-3

DP
type: SiteQuality
SIO_000300: 1.572268e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.13e0

GenotypeDepth
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variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11414
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.014318010550113e-5
allele num: 66350
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10368
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

FS
type: SiteQuality
SIO_000300: 9.327e0

QD
type: SiteQuality
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BaseQRankSum
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SIO_000300: -2.53e-1

VQSLOD
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SIO_000300: -2.562e-1

InbreedingCoeff
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SIO_000300: 1.5e-3

MQ
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SIO_000300: 5.963e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

ClippingRankSum
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SIO_000300: -1.03e-1

MQRankSum
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SIO_000300: 1.11e-1

DP
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SIO_000300: 1.564932e6

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1666
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11414
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16474
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.014318010550113e-5
allele num: 66350
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.03e-1

QD
type: SiteQuality
SIO_000300: 1.091e1

MQ
type: SiteQuality
SIO_000300: 5.963e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

FS
type: SiteQuality
SIO_000300: 9.327e0

DP
type: SiteQuality
SIO_000300: 1.564932e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.53e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.562e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.11e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 5

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10348
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11394
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.046180090166931e-4
allele num: 16414
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66248
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 8.090000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.4e-1

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.79e-1

DP
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SIO_000300: 1.555428e6

BaseQRankSum
type: SiteQuality
SIO_000300: 7.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.33e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10348
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11394
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.038647342995169e-5
allele num: 66240
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

FS
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.555745e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.81e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.264e0

GenotypeDepth
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variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509661835748792e-5
allele num: 66240
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.34e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.49e-1

DP
type: SiteQuality
SIO_000300: 1.554474e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

QD
type: SiteQuality
SIO_000300: 1.244e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.81e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.76e-1

GenotypeDepth
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bin: 1.25e1
variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6560
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8566
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: 1
allele frequency: 9.671179883945841e-5
allele num: 10340
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66198
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.89e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.1e-2

BaseQRankSum
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SIO_000300: 3.69e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.548329e6

InbreedingCoeff
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SIO_000300: 2.0e-3

FS
type: SiteQuality
SIO_000300: 1.786e0

ReadPosRankSum
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SIO_000300: -5.35e-1

ClippingRankSum
type: SiteQuality
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11390
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6560
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66196
num of homozygotes: 0

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

African
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allele count: 1
allele frequency: 9.667440061871617e-5
allele num: 10344
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

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.83e-1

DP
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SIO_000300: 1.548247e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.89e-1

FS
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SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 8.400000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: 7.48e-1

InbreedingCoeff
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SIO_000300: 2.4e-3

QD
type: SiteQuality
SIO_000300: 1.038e1

BaseQRankSum
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SIO_000300: 4.92e0

GenotypeDepth
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variant carriers: 0

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

South Asian
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allele count: 1
allele frequency: 6.1020258725897e-5
allele num: 16388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66196
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6560
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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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

MQ
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SIO_000300: 6.0e1

QD
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VQSLOD
type: SiteQuality
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ReadPosRankSum
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FS
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DP
type: SiteQuality
SIO_000300: 1.548247e6

ClippingRankSum
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SIO_000300: 7.89e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.400000000000001e-2

BaseQRankSum
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SIO_000300: 4.92e0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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allele count: 1
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allele num: 11384
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: 0
allele frequency: 0.0e0
allele num: 66178
num of homozygotes: 0

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

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

East Asian
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num of homozygotes: 0

South Asian
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Latino
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African
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European (Non-Finnish)
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European (Finnish)
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Other
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VQSLOD
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SIO_000300: 1.05e0

DP
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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FS
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MQRankSum
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MQ
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ClippingRankSum
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QD
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SIO_000300: 1.33e1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.022243713733075e-5
allele num: 66176
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 count: 0
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num of homozygotes: 0

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

Other
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East Asian
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allele count: 0
allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
SIO_000300: 1.05e0

QD
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SIO_000300: 1.33e1

DP
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SIO_000300: 1.546237e6

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

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

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

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

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

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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African
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South Asian
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DP
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SIO_000300: 1.52072e6

ClippingRankSum
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MQRankSum
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FS
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MQ
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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QD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 num: 8542
num of homozygotes: 0

South Asian
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European (Finnish)
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Latino
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African
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Other
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European (Non-Finnish)
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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MQ
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FS
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VQSLOD
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BaseQRankSum
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QD
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MQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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European (Non-Finnish)
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African
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Other
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European (Finnish)
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Latino
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MQRankSum
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VQSLOD
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FS
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ReadPosRankSum
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InbreedingCoeff
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QD
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MQ
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DP
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BaseQRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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South Asian
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European (Finnish)
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Latino
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East Asian
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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FS
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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QD
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MQ
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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European (Finnish)
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African
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South Asian
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European (Non-Finnish)
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Other
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DP
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VQSLOD
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FS
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SIO_000300: 1.103e0

MQRankSum
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InbreedingCoeff
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SIO_000300: 1.8e-3

ClippingRankSum
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SIO_000300: -1.66e-1

ReadPosRankSum
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SIO_000300: 1.3e-1

MQ
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SIO_000300: 5.979e1

BaseQRankSum
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QD
type: SiteQuality
SIO_000300: 2.081e1

GenotypeDepth
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8418
num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 8.8999644001424e-5
allele num: 11236
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
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QD
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FS
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DP
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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ClippingRankSum
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SIO_000300: -5.01e-1

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

Latino
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allele frequency: 8.874689385871494e-5
allele num: 11268
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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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66210
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8478
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 3.05e-1

ClippingRankSum
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SIO_000300: -3.55e-1

VQSLOD
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QD
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BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.959e1

FS
type: SiteQuality
SIO_000300: 2.817e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e-1

DP
type: SiteQuality
SIO_000300: 1.869731e6

InbreedingCoeff
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SIO_000300: 3.3e-3

GenotypeDepth
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variant carriers: 0

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 2
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allele num: 16412
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66272
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 4.41e-1

MQ
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SIO_000300: 6.0e1

FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 1.91e-1

BaseQRankSum
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ReadPosRankSum
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SIO_000300: 3.11e-1

DP
type: SiteQuality
SIO_000300: 1.874615e6

MQRankSum
type: SiteQuality
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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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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 9.632055480639569e-5
allele num: 10382
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

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

Latino
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num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

Latino
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European (Non-Finnish)
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African
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East Asian
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Other
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European (Finnish)
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MQ
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ReadPosRankSum
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QD
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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FS
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VQSLOD
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DP
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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Latino
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allele frequency: 0.0e0
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Other
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European (Non-Finnish)
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European (Finnish)
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African
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allele num: 10390
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MQRankSum
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QD
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VQSLOD
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DP
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BaseQRankSum
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FS
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ReadPosRankSum
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MQ
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GenotypeQuality
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African
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MQ
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FS
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European (Non-Finnish)
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DP
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MQ
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VQSLOD
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FS
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QD
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DP
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MQ
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VQSLOD
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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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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10400
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.501501501501501e-5
allele num: 66600
num of homozygotes: 0

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

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

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

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

ClippingRankSum
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SIO_000300: 2.86e-1

MQRankSum
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QD
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FS
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VQSLOD
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SIO_000300: 3.95e-1

BaseQRankSum
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SIO_000300: 4.44e-1

DP
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SIO_000300: 1.89468e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.35e-1

MQ
type: SiteQuality
SIO_000300: 5.98e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

GenotypeDepth
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variant carriers: 1

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66620
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11414
num of homozygotes: 0

African
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allele count: 3
allele frequency: 2.884060757546626e-4
allele num: 10402
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

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

MQ
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SIO_000300: 5.901e1

VQSLOD
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DP
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SIO_000300: 1.895348e6

ClippingRankSum
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MQRankSum
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SIO_000300: 1.02e0

BaseQRankSum
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FS
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SIO_000300: 7.84e-1

InbreedingCoeff
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SIO_000300: -2.0e-4

ReadPosRankSum
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SIO_000300: -5.77e-1

QD
type: SiteQuality
SIO_000300: 9.390000000000001e0

GenotypeDepth
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variant carriers: 5

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 10

GenotypeDepth
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variant carriers: 8

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

South Asian
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allele count: 114
allele frequency: 6.908253545024845e-3
allele num: 16502
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66638
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11430
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.8e0

MQRankSum
type: SiteQuality
SIO_000300: 1.1e-2

ClippingRankSum
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SIO_000300: -8.599999999999999e-2

MQ
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SIO_000300: 5.979e1

VQSLOD
type: SiteQuality
SIO_000300: 5.56e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.35e-1

InbreedingCoeff
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SIO_000300: -5.0e-4

QD
type: SiteQuality
SIO_000300: 1.339e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.90076e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 904
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11430
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500645277469312e-5
allele num: 66638
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
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InbreedingCoeff
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SIO_000300: -5.0e-4

ReadPosRankSum
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MQRankSum
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BaseQRankSum
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MQ
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VQSLOD
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FS
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QD
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ClippingRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8620
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11430
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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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 count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 1
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allele num: 16504
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QD
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FS
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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MQ
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MQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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Latino
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European (Finnish)
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African
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East Asian
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European (Non-Finnish)
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ClippingRankSum
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VQSLOD
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QD
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ReadPosRankSum
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DP
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MQ
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InbreedingCoeff
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FS
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BaseQRankSum
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MQRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Latino
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African
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Other
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South Asian
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European (Finnish)
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FS
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QD
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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DP
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ReadPosRankSum
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MQRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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East Asian
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Latino
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European (Finnish)
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Other
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DP
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MQRankSum
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VQSLOD
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FS
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QD
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InbreedingCoeff
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MQ
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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South Asian
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African
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European (Non-Finnish)
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European (Finnish)
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ReadPosRankSum
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FS
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MQ
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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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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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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European (Non-Finnish)
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European (Finnish)
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African
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South Asian
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East Asian
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Other
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FS
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MQ
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VQSLOD
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MQRankSum
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InbreedingCoeff
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DP
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ClippingRankSum
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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Latino
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Other
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South Asian
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ReadPosRankSum
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QD
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BaseQRankSum
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FS
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InbreedingCoeff
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VQSLOD
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MQRankSum
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ClippingRankSum
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MQ
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DP
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GenotypeDepth
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GenotypeQuality
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Other
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East Asian
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European (Finnish)
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African
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66706
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
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MQ
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SIO_000300: 5.931e1

ClippingRankSum
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InbreedingCoeff
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VQSLOD
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DP
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SIO_000300: 1.897332e6

BaseQRankSum
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SIO_000300: -1.533e0

ReadPosRankSum
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SIO_000300: 1.29e0

FS
type: SiteQuality
SIO_000300: 4.861e0

QD
type: SiteQuality
SIO_000300: 8.359999999999999e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 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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num of homozygotes: 0

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

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

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

South Asian
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allele frequency: 0.0e0
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VQSLOD
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BaseQRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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QD
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MQ
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DP
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SIO_000300: 1.897332e6

GenotypeDepth
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variant carriers: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10402
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
allele num: 66708
num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

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

DP
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SIO_000300: 1.897365e6

VQSLOD
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SIO_000300: -5.158e-1

InbreedingCoeff
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SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 6.860000000000001e-1

ReadPosRankSum
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SIO_000300: 1.21e0

BaseQRankSum
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SIO_000300: 1.22e0

MQRankSum
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SIO_000300: -3.72e-1

QD
type: SiteQuality
SIO_000300: 9.789999999999999e0

MQ
type: SiteQuality
SIO_000300: 5.889e1

ClippingRankSum
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SIO_000300: -1.76e0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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variant carriers: 8

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

European (Non-Finnish)
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allele count: 13
allele frequency: 1.948791749115548e-4
allele num: 66708
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11462
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
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South Asian
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Other
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BaseQRankSum
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SIO_000300: -1.027e0

VQSLOD
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InbreedingCoeff
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FS
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SIO_000300: 5.28e-1

MQRankSum
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ReadPosRankSum
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DP
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ClippingRankSum
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MQ
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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

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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Latino
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African
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East Asian
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Other
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European (Finnish)
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MQRankSum
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VQSLOD
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FS
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DP
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ReadPosRankSum
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InbreedingCoeff
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MQ
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ClippingRankSum
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BaseQRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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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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East Asian
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European (Finnish)
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South Asian
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Latino
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African
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European (Non-Finnish)
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InbreedingCoeff
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QD
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ReadPosRankSum
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BaseQRankSum
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DP
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MQRankSum
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FS
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VQSLOD
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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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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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
all individuals: 11
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33706
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8651
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2909
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 98
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1358
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2388
bin: 8.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499160470136723e-5
allele num: 66704
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11464
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.975e1

VQSLOD
type: SiteQuality
SIO_000300: 1.29e0

DP
type: SiteQuality
SIO_000300: 1.897354e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.57e-1

QD
type: SiteQuality
SIO_000300: 1.208e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.8e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.904e0