18-32438313-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32438313
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32438313
    reference: chr 18
allele count: 1
allele frequency: 8.28239659427852e-6
allele num: 120738
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1336G>C
  hgvsp: ENSP00000470152.1:p.Glu446Gln
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.382G>C
  hgvsp: ENSP00000471783.1:p.Glu128Gln
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000468262
  ensembl transcript: ENST00000587723
  gene symbol: DTNA
  hgvsc: ENST00000587723.1:c.313G>C
  hgvsp: ENSP00000468262.1:p.Glu105Gln
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.472G>C
  hgvsp: ENSP00000452255.2:p.Glu158Gln
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1516G>C
  hgvsp: ENSP00000269191.6:p.Glu506Gln
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1516G>C
  hgvsp: ENSP00000382064.3:p.Glu506Gln
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1507G>C
  hgvsp: ENSP00000336682.4:p.Glu503Gln
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.460G>C
  hgvsp: ENSP00000467720.1:p.Glu154Gln
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.643G>C
  hgvsp: ENSP00000269192.7:p.Glu215Gln
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1345G>C
  hgvsp: ENSP00000470716.1:p.Glu449Gln
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1336G>C
  hgvsp: ENSP00000473119.1:p.Glu446Gln
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.382G>C
  hgvsp: ENSP00000470247.1:p.Glu128Gln
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.460G>C
  hgvsp: ENSP00000382048.3:p.Glu154Gln
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1516G>C
  hgvsp: ENSP00000405819.1:p.Glu506Gln
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1336G>C
  hgvsp: ENSP00000382072.5:p.Glu446Gln
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1345G>C
  hgvsp: ENSP00000283365.9:p.Glu449Gln
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1345G>C
  hgvsp: ENSP00000472031.1:p.Glu449Gln
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.766G>C
  hgvsp: ENSP00000469121.1:p.Glu256Gln
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1519G>C
  hgvsp: ENSP00000269190.7:p.Glu507Gln
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Glu446Gln
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: G
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

18-32438314-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32438314
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32438314
    reference: chr 18
allele count: 1
allele frequency: 8.282533792737874e-6
allele num: 120736
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.383A>T
  hgvsp: ENSP00000470934.1:p.Glu128Val
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000468262
  ensembl transcript: ENST00000587723
  gene symbol: DTNA
  hgvsc: ENST00000587723.1:c.314A>T
  hgvsp: ENSP00000468262.1:p.Glu105Val
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1346A>T
  hgvsp: ENSP00000470716.1:p.Glu449Val
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1346A>T
  hgvsp: ENSP00000472031.1:p.Glu449Val
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1337A>T
  hgvsp: ENSP00000470152.1:p.Glu446Val
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.461A>T
  hgvsp: ENSP00000382048.3:p.Glu154Val
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1337A>T
  hgvsp: ENSP00000473078.1:p.Glu446Val
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1517A>T
  hgvsp: ENSP00000382064.3:p.Glu506Val
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.473A>T
  hgvsp: ENSP00000452255.2:p.Glu158Val
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1520A>T
  hgvsp: ENSP00000269190.7:p.Glu507Val
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1517A>T
  hgvsp: ENSP00000269191.6:p.Glu506Val
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.383A>T
  hgvsp: ENSP00000470247.1:p.Glu128Val
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1508A>T
  hgvsp: ENSP00000336682.4:p.Glu503Val
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.767A>T
  hgvsp: ENSP00000469121.1:p.Glu256Val
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1517A>T
  hgvsp: ENSP00000405819.1:p.Glu506Val
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1337A>T
  hgvsp: ENSP00000382072.5:p.Glu446Val
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1337A>T
  hgvsp: ENSP00000473119.1:p.Glu446Val
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.461A>T
  hgvsp: ENSP00000467720.1:p.Glu154Val
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.644A>T
  hgvsp: ENSP00000269192.7:p.Glu215Val
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Glu446Val
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

18-32438319-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32438319
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32438319
    reference: chr 18
allele count: 1
allele frequency: 8.284043275842073e-6
allele num: 120714
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1522G>A
  hgvsp: ENSP00000382064.3:p.Ala508Thr
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1342G>A
  hgvsp: ENSP00000473078.1:p.Ala448Thr
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1342G>A
  hgvsp: ENSP00000473119.1:p.Ala448Thr
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1351G>A
  hgvsp: ENSP00000470716.1:p.Ala451Thr
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.388G>A
  hgvsp: ENSP00000470934.1:p.Ala130Thr
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000468262
  ensembl transcript: ENST00000587723
  gene symbol: DTNA
  hgvsc: ENST00000587723.1:c.319G>A
  hgvsp: ENSP00000468262.1:p.Ala107Thr
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.478G>A
  hgvsp: ENSP00000452255.2:p.Ala160Thr
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1522G>A
  hgvsp: ENSP00000269191.6:p.Ala508Thr
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.466G>A
  hgvsp: ENSP00000467720.1:p.Ala156Thr
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1522G>A
  hgvsp: ENSP00000405819.1:p.Ala508Thr
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.388G>A
  hgvsp: ENSP00000471783.1:p.Ala130Thr
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1342G>A
  hgvsp: ENSP00000470152.1:p.Ala448Thr
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1342G>A
  hgvsp: ENSP00000382072.5:p.Ala448Thr
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.466G>A
  hgvsp: ENSP00000382048.3:p.Ala156Thr
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1513G>A
  hgvsp: ENSP00000336682.4:p.Ala505Thr
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1351G>A
  hgvsp: ENSP00000472031.1:p.Ala451Thr
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1525G>A
  hgvsp: ENSP00000269190.7:p.Ala509Thr
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.772G>A
  hgvsp: ENSP00000469121.1:p.Ala258Thr
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.649G>A
  hgvsp: ENSP00000269192.7:p.Ala217Thr
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala448Thr
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQRankSum

18-32438329-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32438329
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32438329
    reference: chr 18
allele count: 1
allele frequency: 8.290774026663129e-6
allele num: 120616
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.398A>G
  hgvsp: ENSP00000470247.1:p.Asn133Ser
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.398A>G
  hgvsp: ENSP00000471783.1:p.Asn133Ser
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1352A>G
  hgvsp: ENSP00000473119.1:p.Asn451Ser
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.782A>G
  hgvsp: ENSP00000469121.1:p.Asn261Ser
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.659A>G
  hgvsp: ENSP00000269192.7:p.Asn220Ser
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1352A>G
  hgvsp: ENSP00000470152.1:p.Asn451Ser
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1535A>G
  hgvsp: ENSP00000269190.7:p.Asn512Ser
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1523A>G
  hgvsp: ENSP00000336682.4:p.Asn508Ser
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.476A>G
  hgvsp: ENSP00000382048.3:p.Asn159Ser
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1361A>G
  hgvsp: ENSP00000470716.1:p.Asn454Ser
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1361A>G
  hgvsp: ENSP00000472031.1:p.Asn454Ser
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1352A>G
  hgvsp: ENSP00000473078.1:p.Asn451Ser
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.398A>G
  hgvsp: ENSP00000470934.1:p.Asn133Ser
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.488A>G
  hgvsp: ENSP00000452255.2:p.Asn163Ser
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.476A>G
  hgvsp: ENSP00000467720.1:p.Asn159Ser
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1532A>G
  hgvsp: ENSP00000382064.3:p.Asn511Ser
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1532A>G
  hgvsp: ENSP00000405819.1:p.Asn511Ser
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1352A>G
  hgvsp: ENSP00000382072.5:p.Asn451Ser
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1532A>G
  hgvsp: ENSP00000269191.6:p.Asn511Ser
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asn451Ser
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/18-32438333-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32438333
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32438333
    reference: chr 18
allele count: 1
allele frequency: 8.29393713195654e-6
allele num: 120570
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1356C>A
  hgvsp: ENST00000595022.1:c.1356C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1365C>A
  hgvsp: ENST00000598774.1:c.1365C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1536C>A
  hgvsp: ENST00000444659.1:c.1536C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.492C>A
  hgvsp: ENST00000556414.3:c.492C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1539C>A
  hgvsp: ENST00000269190.7:c.1539C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1365C>A
  hgvsp: ENST00000598142.1:c.1365C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.480C>A
  hgvsp: ENST00000399097.3:c.480C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1356C>A
  hgvsp: ENST00000597599.1:c.1356C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.786C>A
  hgvsp: ENST00000596745.1:c.786C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.402C>A
  hgvsp: ENST00000599844.1:c.402C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1356C>A
  hgvsp: ENST00000598334.1:c.1356C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1536C>A
  hgvsp: ENST00000399113.3:c.1536C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.480C>A
  hgvsp: ENST00000591182.1:c.480C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.402C>A
  hgvsp: ENST00000597674.1:c.402C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1527C>A
  hgvsp: ENST00000348997.5:c.1527C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1536C>A
  hgvsp: ENST00000269191.6:c.1536C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1356C>A
  hgvsp: ENST00000399121.5:c.1356C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.663C>A
  hgvsp: ENST00000269192.7:c.663C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1365C>A
  hgvsp: ENST00000283365.9:c.1365C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro452Pro
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

18-32438333-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32438333
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32438333
    reference: chr 18
allele count: 1
allele frequency: 8.29393713195654e-6
allele num: 120570
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1356C>G
  hgvsp: ENST00000598334.1:c.1356C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1536C>G
  hgvsp: ENST00000399113.3:c.1536C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1527C>G
  hgvsp: ENST00000348997.5:c.1527C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1536C>G
  hgvsp: ENST00000444659.1:c.1536C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1356C>G
  hgvsp: ENST00000399121.5:c.1356C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.480C>G
  hgvsp: ENST00000591182.1:c.480C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.402C>G
  hgvsp: ENST00000599844.1:c.402C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1539C>G
  hgvsp: ENST00000269190.7:c.1539C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1536C>G
  hgvsp: ENST00000269191.6:c.1536C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1365C>G
  hgvsp: ENST00000598774.1:c.1365C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.402C>G
  hgvsp: ENST00000597674.1:c.402C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.663C>G
  hgvsp: ENST00000269192.7:c.663C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.480C>G
  hgvsp: ENST00000399097.3:c.480C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.492C>G
  hgvsp: ENST00000556414.3:c.492C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1365C>G
  hgvsp: ENST00000598142.1:c.1365C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.786C>G
  hgvsp: ENST00000596745.1:c.786C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1356C>G
  hgvsp: ENST00000595022.1:c.1356C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1356C>G
  hgvsp: ENST00000597599.1:c.1356C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.402C>G
  hgvsp: ENST00000601125.1:c.402C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro452Pro
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

18-32438335-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32438335
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32438335
    reference: chr 18
allele count: 1
allele frequency: 8.297102651754007e-6
allele num: 120524
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1358C>T
  hgvsp: ENSP00000470152.1:p.Thr453Ile
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1358C>T
  hgvsp: ENSP00000473119.1:p.Thr453Ile
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.404C>T
  hgvsp: ENSP00000471783.1:p.Thr135Ile
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1358C>T
  hgvsp: ENSP00000382072.5:p.Thr453Ile
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1529C>T
  hgvsp: ENSP00000336682.4:p.Thr510Ile
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.494C>T
  hgvsp: ENSP00000452255.2:p.Thr165Ile
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1538C>T
  hgvsp: ENSP00000405819.1:p.Thr513Ile
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1367C>T
  hgvsp: ENSP00000472031.1:p.Thr456Ile
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1367C>T
  hgvsp: ENSP00000283365.9:p.Thr456Ile
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1541C>T
  hgvsp: ENSP00000269190.7:p.Thr514Ile
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.482C>T
  hgvsp: ENSP00000382048.3:p.Thr161Ile
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1367C>T
  hgvsp: ENSP00000470716.1:p.Thr456Ile
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.482C>T
  hgvsp: ENSP00000467720.1:p.Thr161Ile
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1538C>T
  hgvsp: ENSP00000269191.6:p.Thr513Ile
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1358C>T
  hgvsp: ENSP00000473078.1:p.Thr453Ile
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.404C>T
  hgvsp: ENSP00000470934.1:p.Thr135Ile
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.788C>T
  hgvsp: ENSP00000469121.1:p.Thr263Ile
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1538C>T
  hgvsp: ENSP00000382064.3:p.Thr513Ile
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.665C>T
  hgvsp: ENSP00000269192.7:p.Thr222Ile
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Thr453Ile
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: African
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

18-32438352-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32438352
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32438352
    reference: chr 18
allele count: 1
allele frequency: 8.336807002917883e-6
allele num: 119950
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1555C>T
  hgvsp: ENSP00000405819.1:p.Arg519Trp
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.499C>T
  hgvsp: ENSP00000382048.3:p.Arg167Trp
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.805C>T
  hgvsp: ENSP00000469121.1:p.Arg269Trp
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1375C>T
  hgvsp: ENSP00000473119.1:p.Arg459Trp
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.499C>T
  hgvsp: ENSP00000467720.1:p.Arg167Trp
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1384C>T
  hgvsp: ENSP00000283365.9:p.Arg462Trp
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.421C>T
  hgvsp: ENSP00000471783.1:p.Arg141Trp
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1384C>T
  hgvsp: ENSP00000470716.1:p.Arg462Trp
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1555C>T
  hgvsp: ENSP00000382064.3:p.Arg519Trp
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.421C>T
  hgvsp: ENSP00000470247.1:p.Arg141Trp
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1546C>T
  hgvsp: ENSP00000336682.4:p.Arg516Trp
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1375C>T
  hgvsp: ENSP00000470152.1:p.Arg459Trp
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1375C>T
  hgvsp: ENSP00000382072.5:p.Arg459Trp
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.511C>T
  hgvsp: ENSP00000452255.2:p.Arg171Trp
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1558C>T
  hgvsp: ENSP00000269190.7:p.Arg520Trp
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.421C>T
  hgvsp: ENSP00000470934.1:p.Arg141Trp
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.682C>T
  hgvsp: ENSP00000269192.7:p.Arg228Trp
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1555C>T
  hgvsp: ENSP00000269191.6:p.Arg519Trp
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1375C>T
  hgvsp: ENSP00000473078.1:p.Arg459Trp
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg459Trp
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD

18-32438354-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32438354
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32438354
    reference: chr 18
allele count: 1
allele frequency: 8.343484572897024e-6
allele num: 119854
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.501G>A
  hgvsp: ENST00000399097.3:c.501G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1377G>A
  hgvsp: ENST00000399121.5:c.1377G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1377G>A
  hgvsp: ENST00000597599.1:c.1377G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.423G>A
  hgvsp: ENST00000601125.1:c.423G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1557G>A
  hgvsp: ENST00000444659.1:c.1557G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.684G>A
  hgvsp: ENST00000269192.7:c.684G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1548G>A
  hgvsp: ENST00000348997.5:c.1548G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.513G>A
  hgvsp: ENST00000556414.3:c.513G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1386G>A
  hgvsp: ENST00000283365.9:c.1386G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1377G>A
  hgvsp: ENST00000595022.1:c.1377G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.501G>A
  hgvsp: ENST00000591182.1:c.501G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1560G>A
  hgvsp: ENST00000269190.7:c.1560G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1377G>A
  hgvsp: ENST00000598334.1:c.1377G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.807G>A
  hgvsp: ENST00000596745.1:c.807G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1386G>A
  hgvsp: ENST00000598142.1:c.1386G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1557G>A
  hgvsp: ENST00000269191.6:c.1557G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1557G>A
  hgvsp: ENST00000399113.3:c.1557G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.423G>A
  hgvsp: ENST00000599844.1:c.423G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.423G>A
  hgvsp: ENST00000597674.1:c.423G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg459Arg
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff

18-32438355-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32438355
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32438355
    reference: chr 18
allele count: 1
allele frequency: 8.346688034188035e-6
allele num: 119808
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.808C>T
  hgvsp: ENSP00000469121.1:p.Leu270Phe
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1387C>T
  hgvsp: ENSP00000472031.1:p.Leu463Phe
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1558C>T
  hgvsp: ENSP00000382064.3:p.Leu520Phe
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1561C>T
  hgvsp: ENSP00000269190.7:p.Leu521Phe
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1558C>T
  hgvsp: ENSP00000269191.6:p.Leu520Phe
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.685C>T
  hgvsp: ENSP00000269192.7:p.Leu229Phe
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1378C>T
  hgvsp: ENSP00000382072.5:p.Leu460Phe
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1558C>T
  hgvsp: ENSP00000405819.1:p.Leu520Phe
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.424C>T
  hgvsp: ENSP00000470247.1:p.Leu142Phe
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1387C>T
  hgvsp: ENSP00000470716.1:p.Leu463Phe
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.502C>T
  hgvsp: ENSP00000382048.3:p.Leu168Phe
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1378C>T
  hgvsp: ENSP00000470152.1:p.Leu460Phe
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1378C>T
  hgvsp: ENSP00000473119.1:p.Leu460Phe
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.502C>T
  hgvsp: ENSP00000467720.1:p.Leu168Phe
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1378C>T
  hgvsp: ENSP00000473078.1:p.Leu460Phe
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.514C>T
  hgvsp: ENSP00000452255.2:p.Leu172Phe
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.424C>T
  hgvsp: ENSP00000471783.1:p.Leu142Phe
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1549C>T
  hgvsp: ENSP00000336682.4:p.Leu517Phe
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1387C>T
  hgvsp: ENSP00000283365.9:p.Leu463Phe
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu460Phe
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

18-32438366-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32438366
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32438366
    reference: chr 18
allele count: 12
allele frequency: 1.008335574079054e-4
allele num: 119008
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.431+4G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1556+4G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.431+4G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1394+4G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.521+4G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1394+4G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.509+4G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.692+4G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1568+4G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1565+4G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1385+4G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1385+4G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.509+4G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1565+4G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.431+4G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1385+4G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1565+4G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1394+4G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.815+4G>A
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.1385+4G>A
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

18-32438373-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32438373
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32438373
    reference: chr 18
allele count: 1
allele frequency: 8.463530646444471e-6
allele num: 118154
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1556+11G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.431+11G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.692+11G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.815+11G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1385+11G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.431+11G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1385+11G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1565+11G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1385+11G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1565+11G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1568+11G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.509+11G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1394+11G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.509+11G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.431+11G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1394+11G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1385+11G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1394+11G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.521+11G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1565+11G>C
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP

18-32438379-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32438379
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32438379
    reference: chr 18
allele count: 2
allele frequency: 1.707650273224044e-5
allele num: 117120
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.509+17A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1385+17A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.815+17A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.509+17A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1385+17A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.692+17A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.521+17A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.431+17A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.431+17A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1565+17A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1394+17A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1556+17A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1385+17A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1385+17A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1394+17A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.431+17A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1394+17A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1565+17A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1565+17A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1568+17A>G
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6946
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

18-32438379-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32438379
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32438379
    reference: chr 18
allele count: 2
allele frequency: 1.707650273224044e-5
allele num: 117120
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1568+17A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.431+17A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1385+17A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1394+17A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1394+17A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.431+17A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1565+17A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1394+17A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.431+17A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1556+17A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.509+17A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.521+17A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1385+17A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.509+17A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1385+17A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1565+17A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.815+17A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1565+17A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1385+17A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.692+17A>T
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

18-32438401-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32438401
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32438401
    reference: chr 18
allele count: 1
allele frequency: 8.735608085678845e-6
allele num: 114474
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1565+39T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1385+39T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.509+39T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1385+39T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.815+39T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.431+39T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1394+39T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1565+39T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1568+39T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.431+39T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.509+39T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1385+39T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1556+39T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1385+39T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.521+39T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1394+39T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1394+39T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.692+39T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.431+39T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1565+39T>C
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP

18-32443880-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32443880
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32443880
    reference: chr 18
allele count: 1
allele frequency: 2.043067870714665e-5
allele num: 48946
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.432-50T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1386-50T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.432-50T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.510-50T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1569-50T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1395-50T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1557-50T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1395-50T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1566-50T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.693-50T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1566-50T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.522-50T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1386-50T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.510-50T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1386-50T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1386-50T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1395-50T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.432-54T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1566-50T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.816-50T>C
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

18-32443897-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32443897
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32443897
    reference: chr 18
allele count: 2
allele frequency: 3.88259046435782e-5
allele num: 51512
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1386-33T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1566-33T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1569-33T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1557-33T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1395-33T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.432-33T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1386-33T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.510-33T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.510-33T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.432-33T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1395-33T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1386-33T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1386-33T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.693-33T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1566-33T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.816-33T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.432-37T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1395-33T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.522-33T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1566-33T>C
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQ

18-32443898-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32443898
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32443897
    reference: chr 18
allele count: 42
allele frequency: 8.132915069129778e-4
allele num: 51642
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1386-30delC
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.693-30delC
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1386-30delC
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1566-30delC
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1569-30delC
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1557-30delC
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.510-30delC
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1566-30delC
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.522-30delC
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1395-30delC
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.432-34delC
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.816-30delC
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.510-30delC
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1395-30delC
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1386-30delC
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.432-30delC
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1395-30delC
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1386-30delC
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1566-30delC
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.432-30delC
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4242
  bin: 2.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: GC
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum

18-32443900-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32443900
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32443900
    reference: chr 18
allele count: 2
allele frequency: 3.817959682345755e-5
allele num: 52384
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.693-30C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1395-30C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.522-30C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.510-30C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1395-30C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.432-34C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1395-30C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1566-30C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1566-30C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.510-30C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1557-30C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1569-30C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.816-30C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1386-30C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.432-30C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1386-30C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1386-30C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1386-30C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.432-30C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1566-30C>G
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10707
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ

18-32443900-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32443900
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32443900
    reference: chr 18
allele count: 4
allele frequency: 7.635919364691509e-5
allele num: 52384
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.432-30C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1395-30C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1386-30C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.432-34C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.510-30C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1557-30C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1566-30C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1386-30C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.816-30C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1386-30C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.693-30C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1569-30C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.510-30C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1386-30C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1566-30C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1395-30C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.522-30C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.432-30C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1566-30C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1395-30C>T
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD

18-32443908-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32443908
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32443907
    reference: chr 18
allele count: 0
allele frequency: 0.0e0
allele num: 57428
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1395-21delT
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.510-21delT
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1395-21delT
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1386-21delT
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1569-21delT
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1566-21delT
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.432-21delT
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1566-21delT
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.432-21delT
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1557-21delT
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.522-21delT
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1395-21delT
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1566-21delT
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1386-21delT
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.432-25delT
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.693-21delT
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.816-21delT
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1386-21delT
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.510-21delT
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1386-21delT
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: AT
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

18-32443910-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32443910
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32443910
    reference: chr 18
allele count: 1
allele frequency: 1.708292049608801e-5
allele num: 58538
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.510-20G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1569-20G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1386-20G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1386-20G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1557-20G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1386-20G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.816-20G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1386-20G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1566-20G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.432-20G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1566-20G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1566-20G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1395-20G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1395-20G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.510-20G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.522-20G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.432-24G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.432-20G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.693-20G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1395-20G>A
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD

18-32443918-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32443918
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32443918
    reference: chr 18
allele count: 21
allele frequency: 3.19071350431506e-4
allele num: 65816
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.816-12C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.510-12C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1386-12C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.432-12C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1569-12C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1566-12C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.510-12C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1566-12C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1557-12C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1386-12C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.693-12C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.432-12C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.522-12C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1395-12C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1386-12C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1395-12C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.432-16C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1566-12C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1386-12C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1395-12C>T
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7097
  bin: 1.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

18-32443935-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32443935
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32443935
    reference: chr 18
allele count: 14
allele frequency: 1.724307813577692e-4
allele num: 81192
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.433G>A
  hgvsp: ENSP00000470934.1:p.Ala145Thr
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1571G>A
  hgvsp: ENSP00000382064.3:p.Arg524His
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1391G>A
  hgvsp: ENSP00000382072.5:p.Arg464His
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1400G>A
  hgvsp: ENSP00000472031.1:p.Arg467His
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1391G>A
  hgvsp: ENSP00000470152.1:p.Arg464His
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1400G>A
  hgvsp: ENSP00000283365.9:p.Arg467His
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1571G>A
  hgvsp: ENSP00000269191.6:p.Arg524His
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1574G>A
  hgvsp: ENSP00000269190.7:p.Arg525His
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1571G>A
  hgvsp: ENSP00000405819.1:p.Arg524His
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1562G>A
  hgvsp: ENSP00000336682.4:p.Arg521His
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.515G>A
  hgvsp: ENSP00000382048.3:p.Arg172His
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1391G>A
  hgvsp: ENSP00000473119.1:p.Arg464His
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.437G>A
  hgvsp: ENSP00000470247.1:p.Arg146His
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.437G>A
  hgvsp: ENSP00000471783.1:p.Arg146His
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.698G>A
  hgvsp: ENSP00000269192.7:p.Arg233His
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.527G>A
  hgvsp: ENSP00000452255.2:p.Arg176His
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.821G>A
  hgvsp: ENSP00000469121.1:p.Arg274His
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.515G>A
  hgvsp: ENSP00000467720.1:p.Arg172His
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1400G>A
  hgvsp: ENSP00000470716.1:p.Arg467His
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg464His
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQ

18-32443942-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32443942
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32443942
    reference: chr 18
allele count: 1
allele frequency: 1.132656759695542e-5
allele num: 88288
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1581T>C
  hgvsp: ENST00000269190.7:c.1581T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1398T>C
  hgvsp: ENST00000598334.1:c.1398T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1398T>C
  hgvsp: ENST00000597599.1:c.1398T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1398T>C
  hgvsp: ENST00000595022.1:c.1398T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.522T>C
  hgvsp: ENST00000591182.1:c.522T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.444T>C
  hgvsp: ENST00000597674.1:c.444T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1398T>C
  hgvsp: ENST00000399121.5:c.1398T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1407T>C
  hgvsp: ENST00000598774.1:c.1407T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1569T>C
  hgvsp: ENST00000348997.5:c.1569T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1578T>C
  hgvsp: ENST00000399113.3:c.1578T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.444T>C
  hgvsp: ENST00000601125.1:c.444T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1578T>C
  hgvsp: ENST00000444659.1:c.1578T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1578T>C
  hgvsp: ENST00000269191.6:c.1578T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.534T>C
  hgvsp: ENST00000556414.3:c.534T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1407T>C
  hgvsp: ENST00000283365.9:c.1407T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.440T>C
  hgvsp: ENSP00000470934.1:p.Met147Thr
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.828T>C
  hgvsp: ENST00000596745.1:c.828T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1407T>C
  hgvsp: ENST00000598142.1:c.1407T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.705T>C
  hgvsp: ENST00000269192.7:c.705T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Met147Thr
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
reference allele: T
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ

18-32443954-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32443954
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32443954
    reference: chr 18
allele count: 1
allele frequency: 1.055765535589856e-5
allele num: 94718
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.452G>C
  hgvsp: ENSP00000470934.1:p.Arg151Thr
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1419G>C
  hgvsp: ENSP00000470716.1:p.Gln473His
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.546G>C
  hgvsp: ENSP00000452255.2:p.Gln182His
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1581G>C
  hgvsp: ENSP00000336682.4:p.Gln527His
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1593G>C
  hgvsp: ENSP00000269190.7:p.Gln531His
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1410G>C
  hgvsp: ENSP00000473078.1:p.Gln470His
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1410G>C
  hgvsp: ENSP00000382072.5:p.Gln470His
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.456G>C
  hgvsp: ENSP00000471783.1:p.Gln152His
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1410G>C
  hgvsp: ENSP00000473119.1:p.Gln470His
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1590G>C
  hgvsp: ENSP00000405819.1:p.Gln530His
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.456G>C
  hgvsp: ENSP00000470247.1:p.Gln152His
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.717G>C
  hgvsp: ENSP00000269192.7:p.Gln239His
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1410G>C
  hgvsp: ENSP00000470152.1:p.Gln470His
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1419G>C
  hgvsp: ENSP00000283365.9:p.Gln473His
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.534G>C
  hgvsp: ENSP00000382048.3:p.Gln178His
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.534G>C
  hgvsp: ENSP00000467720.1:p.Gln178His
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1419G>C
  hgvsp: ENSP00000472031.1:p.Gln473His
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1590G>C
  hgvsp: ENSP00000269191.6:p.Gln530His
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1590G>C
  hgvsp: ENSP00000382064.3:p.Gln530His
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gln470His
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Other
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

18-32443978-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32443978
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32443978
    reference: chr 18
allele count: 3
allele frequency: 3.033796492931254e-5
allele num: 98886
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.476C>T
  hgvsp: ENSP00000470934.1:p.Ala159Val
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1614C>T
  hgvsp: ENST00000444659.1:c.1614C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1614C>T
  hgvsp: ENST00000399113.3:c.1614C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1605C>T
  hgvsp: ENST00000348997.5:c.1605C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.480C>T
  hgvsp: ENST00000597674.1:c.480C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1443C>T
  hgvsp: ENST00000598142.1:c.1443C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1434C>T
  hgvsp: ENST00000598334.1:c.1434C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1614C>T
  hgvsp: ENST00000269191.6:c.1614C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1443C>T
  hgvsp: ENST00000598774.1:c.1443C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.558C>T
  hgvsp: ENST00000399097.3:c.558C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.558C>T
  hgvsp: ENST00000591182.1:c.558C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1434C>T
  hgvsp: ENST00000597599.1:c.1434C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1617C>T
  hgvsp: ENST00000269190.7:c.1617C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1434C>T
  hgvsp: ENST00000399121.5:c.1434C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.741C>T
  hgvsp: ENST00000269192.7:c.741C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.570C>T
  hgvsp: ENST00000556414.3:c.570C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1434C>T
  hgvsp: ENST00000595022.1:c.1434C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.864C>T
  hgvsp: ENST00000596745.1:c.864C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.480C>T
  hgvsp: ENST00000601125.1:c.480C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala159Val
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

18-32443984-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32443984
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32443984
    reference: chr 18
allele count: 1
allele frequency: 1.008939201323728e-5
allele num: 99114
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1449A>G
  hgvsp: ENST00000598774.1:c.1449A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1620A>G
  hgvsp: ENST00000269191.6:c.1620A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.747A>G
  hgvsp: ENST00000269192.7:c.747A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1440A>G
  hgvsp: ENST00000598334.1:c.1440A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1620A>G
  hgvsp: ENST00000444659.1:c.1620A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1611A>G
  hgvsp: ENST00000348997.5:c.1611A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.482A>G
  hgvsp: ENSP00000470934.1:p.Glu161Gly
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1623A>G
  hgvsp: ENST00000269190.7:c.1623A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1440A>G
  hgvsp: ENST00000597599.1:c.1440A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1440A>G
  hgvsp: ENST00000399121.5:c.1440A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1449A>G
  hgvsp: ENST00000598142.1:c.1449A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.486A>G
  hgvsp: ENST00000597674.1:c.486A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.576A>G
  hgvsp: ENST00000556414.3:c.576A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1620A>G
  hgvsp: ENST00000399113.3:c.1620A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.870A>G
  hgvsp: ENST00000596745.1:c.870A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.564A>G
  hgvsp: ENST00000591182.1:c.564A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.486A>G
  hgvsp: ENST00000601125.1:c.486A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.564A>G
  hgvsp: ENST00000399097.3:c.564A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1440A>G
  hgvsp: ENST00000595022.1:c.1440A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Glu161Gly
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

18-32444021-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32444021
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32444021
    reference: chr 18
allele count: 1
allele frequency: 1.105998938241019e-5
allele num: 90416
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.784C>T
  hgvsp: ENST00000269192.7:c.784C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1657C>T
  hgvsp: ENST00000399113.3:c.1657C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1648C>T
  hgvsp: ENST00000348997.5:c.1648C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.907C>T
  hgvsp: ENST00000596745.1:c.907C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1477C>T
  hgvsp: ENST00000399121.5:c.1477C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1657C>T
  hgvsp: ENST00000444659.1:c.1657C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1657C>T
  hgvsp: ENST00000269191.6:c.1657C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1660C>T
  hgvsp: ENST00000269190.7:c.1660C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.601C>T
  hgvsp: ENST00000399097.3:c.601C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1486C>T
  hgvsp: ENST00000598774.1:c.1486C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.523C>T
  hgvsp: ENST00000597674.1:c.523C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1477C>T
  hgvsp: ENST00000598334.1:c.1477C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.601C>T
  hgvsp: ENST00000591182.1:c.601C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1486C>T
  hgvsp: ENST00000598142.1:c.1486C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.523C>T
  hgvsp: ENST00000601125.1:c.523C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1477C>T
  hgvsp: ENST00000597599.1:c.1477C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.613C>T
  hgvsp: ENST00000556414.3:c.613C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1486C>T
  hgvsp: ENST00000283365.9:c.1486C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.*30C>T
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu493Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

18-32444023-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32444023
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32444023
    reference: chr 18
allele count: 2
allele frequency: 2.226774739467355e-5
allele num: 89816
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.*32A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1488A>G
  hgvsp: ENST00000598774.1:c.1488A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1659A>G
  hgvsp: ENST00000269191.6:c.1659A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1662A>G
  hgvsp: ENST00000269190.7:c.1662A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.603A>G
  hgvsp: ENST00000399097.3:c.603A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1488A>G
  hgvsp: ENST00000598142.1:c.1488A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.786A>G
  hgvsp: ENST00000269192.7:c.786A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.603A>G
  hgvsp: ENST00000591182.1:c.603A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1479A>G
  hgvsp: ENST00000598334.1:c.1479A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.909A>G
  hgvsp: ENST00000596745.1:c.909A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1479A>G
  hgvsp: ENST00000597599.1:c.1479A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.525A>G
  hgvsp: ENST00000601125.1:c.525A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.525A>G
  hgvsp: ENST00000597674.1:c.525A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.615A>G
  hgvsp: ENST00000556414.3:c.615A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1659A>G
  hgvsp: ENST00000444659.1:c.1659A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1650A>G
  hgvsp: ENST00000348997.5:c.1650A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1479A>G
  hgvsp: ENST00000399121.5:c.1479A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1479A>G
  hgvsp: ENST00000595022.1:c.1479A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1659A>G
  hgvsp: ENST00000399113.3:c.1659A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu493Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD

18-32444035-TGCCAGATAAATTTTCCTGA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32444035
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32444016
    reference: chr 18
allele count: 3
allele frequency: 3.601008282319049e-5
allele num: 83310
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15968
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: TGCCAGATAAATTTTCCTGA
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

18-32444035-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32444035
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32444035
    reference: chr 18
allele count: 1
allele frequency: 1.20033609410635e-5
allele num: 83310
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.528+9T>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1665+9T>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.*35+9T>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1482+9T>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.912+9T>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1482+9T>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1662+9T>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1482+9T>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1491+9T>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.606+9T>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1662+9T>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1491+9T>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.528+9T>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1482+9T>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1491+9T>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.606+9T>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.789+9T>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1662+9T>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.618+9T>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1653+9T>A
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

18-32444039-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32444039
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32444039
    reference: chr 18
allele count: 1
allele frequency: 1.235696809430838e-5
allele num: 80926
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.912+13A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1482+13A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1662+13A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1653+13A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1491+13A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.528+13A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1662+13A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1662+13A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1482+13A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1491+13A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.528+13A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1482+13A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.606+13A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.789+13A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.618+13A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.*35+13A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.606+13A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1665+13A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1491+13A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1482+13A>T
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

18-32444040-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32444040
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32444040
    reference: chr 18
allele count: 29244
allele frequency: 3.585932901706886e-1
allele num: 81552
alternate allele: A
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1491+14G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.606+14G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1653+14G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1482+14G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1482+14G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.912+14G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1662+14G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1491+14G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1482+14G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.528+14G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.528+14G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1665+14G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.618+14G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.606+14G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1491+14G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.*35+14G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1662+14G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1482+14G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1662+14G>A
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 4844
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

18-32444041-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32444041
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32444041
    reference: chr 18
allele count: 3
allele frequency: 4.502881844380403e-5
allele num: 66624
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.912+15A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1491+15A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1482+15A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.*35+15A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1662+15A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1665+15A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.606+15A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.528+15A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.528+15A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1662+15A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.789+15A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.606+15A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1653+15A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1482+15A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1482+15A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1482+15A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1491+15A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1662+15A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.618+15A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1491+15A>T
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

18-32444053-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32444053
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32444053
    reference: chr 18
allele count: 1
allele frequency: 1.786735277301315e-5
allele num: 55968
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.*35+27G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.789+27G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1662+27G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1482+27G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.606+27G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1482+27G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.618+27G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1653+27G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1665+27G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.912+27G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1491+27G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.528+27G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1482+27G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.606+27G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1491+27G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1491+27G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1662+27G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.528+27G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1482+27G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1662+27G>A
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

18-32444055-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32444055
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32444055
    reference: chr 18
allele count: 1
allele frequency: 1.837289630337326e-5
allele num: 54428
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1491+29G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.618+29G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.*35+29G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.606+29G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1482+29G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.528+29G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1491+29G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.606+29G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1491+29G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1482+29G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1665+29G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1482+29G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1662+29G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1662+29G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1482+29G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.789+29G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.912+29G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1653+29G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1662+29G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.528+29G>C
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11092
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum

18-32444073-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32444073
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32444073
    reference: chr 18
allele count: 1
allele frequency: 2.507019655034095e-5
allele num: 39888
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.789+47C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.606+47C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.912+47C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1665+47C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1662+47C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1482+47C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.528+47C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1662+47C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.*35+47C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1482+47C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1653+47C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1491+47C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.528+47C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1662+47C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.606+47C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1491+47C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1482+47C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.618+47C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1491+47C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1482+47C>T
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

18-32444075-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32444075
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32444075
    reference: chr 18
allele count: 0
allele frequency: 0.0e0
allele num: 38896
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.912+49G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1482+49G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1491+49G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1491+49G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.606+49G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.606+49G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.618+49G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1482+49G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.*35+49G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1482+49G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1662+49G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1665+49G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.528+49G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1662+49G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1653+49G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.528+49G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1662+49G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1482+49G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.789+49G>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1491+49G>C
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 8623
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

18-32444077-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32444077
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32444076
    reference: chr 18
allele count: 1
allele frequency: 2.667520273154076e-5
allele num: 37488
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1662+55delA
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.912+55delA
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.618+55delA
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.606+55delA
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.528+55delA
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1482+55delA
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1662+55delA
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1491+55delA
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1665+55delA
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1662+55delA
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.528+55delA
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1482+55delA
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.789+55delA
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1491+55delA
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1482+55delA
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1482+55delA
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1653+55delA
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.606+55delA
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.*35+55delA
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1491+55delA
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: East Asian
reference allele: GA
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

18-32446027-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32446027
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32446027
    reference: chr 18
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1482+2001A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1665+2001A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1492-48A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1483-48A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.618+2001A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.*36-48A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.606+2001A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1483-48A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.528+2001A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1482+2001A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1663-48A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1654-48A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.529-48A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.913-48A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.789+2001A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1662+2001A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.606+2001A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1491+2001A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1491+2001A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1662+2001A>G
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/18-32446034-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32446034
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32446034
    reference: chr 18
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1663-41C>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.*36-41C>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1662+2008C>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1662+2008C>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.529-41C>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1483-41C>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.606+2008C>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1483-41C>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1654-41C>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1482+2008C>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1491+2008C>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1482+2008C>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1492-41C>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.913-41C>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1491+2008C>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.618+2008C>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.606+2008C>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.789+2008C>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.528+2008C>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1665+2008C>A
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3795
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ

http://identifiers.org/exac.variant/18-32446042-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32446042
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32446042
    reference: chr 18
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1663-33A>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.529-33A>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1492-33A>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1483-33A>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.528+2016A>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1654-33A>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.*36-33A>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1491+2016A>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1483-33A>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.606+2016A>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1662+2016A>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1665+2016A>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1482+2016A>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.913-33A>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1662+2016A>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1491+2016A>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.618+2016A>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.606+2016A>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1482+2016A>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.789+2016A>C
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

18-32446049-CTG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32446049
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32446047
    reference: chr 18
allele count: 4
allele frequency: 3.294675803900896e-5
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1482+2025_1482+2026delGT
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1482+2025_1482+2026delGT
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.606+2025_606+2026delGT
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.789+2025_789+2026delGT
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1491+2025_1491+2026delGT
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.528+2025_528+2026delGT
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1654-24_1654-23delGT
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.529-24_529-23delGT
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1665+2025_1665+2026delGT
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1483-24_1483-23delGT
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1492-24_1492-23delGT
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.913-24_913-23delGT
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1662+2025_1662+2026delGT
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1491+2025_1491+2026delGT
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1662+2025_1662+2026delGT
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.*36-24_*36-23delGT
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1663-24_1663-23delGT
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1483-24_1483-23delGT
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.606+2025_606+2026delGT
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.618+2025_618+2026delGT
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: CTG
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD

18-32446052-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32446052
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32446052
    reference: chr 18
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1492-23T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.606+2026T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1654-23T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.913-23T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1662+2026T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.529-23T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.*36-23T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1483-23T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.789+2026T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1483-23T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.606+2026T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1663-23T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1665+2026T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1482+2026T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1491+2026T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1662+2026T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.618+2026T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1482+2026T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1491+2026T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.528+2026T>C
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16812
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD

18-32446055-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32446055
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32446055
    reference: chr 18
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1662+2029T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1665+2029T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.529-20T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1654-20T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.789+2029T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1662+2029T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1483-20T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1482+2029T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1483-20T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1492-20T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1663-20T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.618+2029T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1482+2029T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.606+2029T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.528+2029T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1491+2029T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1491+2029T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.913-20T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.*36-20T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.606+2029T>C
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP

18-32446057-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32446057
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32446057
    reference: chr 18
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.789+2031G>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.606+2031G>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1482+2031G>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1654-18G>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1492-18G>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.606+2031G>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1491+2031G>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1662+2031G>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1491+2031G>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.528+2031G>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1482+2031G>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1663-18G>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1483-18G>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.913-18G>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.*36-18G>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1662+2031G>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1665+2031G>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.529-18G>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1483-18G>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.618+2031G>T
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS

18-32446063-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32446063
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32446063
    reference: chr 18
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1482+2037A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.618+2037A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1663-12A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.789+2037A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.606+2037A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1483-12A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1491+2037A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1665+2037A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1662+2037A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.606+2037A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1492-12A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.529-12A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1491+2037A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1654-12A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1483-12A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.913-12A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1662+2037A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.*36-12A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.528+2037A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1482+2037A>G
  variant of: http://identifiers.org/hgnc/3057
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: African
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

18-32446070-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32446070
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32446070
    reference: chr 18
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.618+2044T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.606+2044T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1663-5T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1483-5T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.529-5T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1662+2044T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.528+2044T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1662+2044T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.913-5T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.606+2044T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1491+2044T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.789+2044T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1482+2044T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1482+2044T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1483-5T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.*36-5T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1654-5T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1491+2044T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1665+2044T>C
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1492-5T>C
  variant of: http://identifiers.org/hgnc/3057
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.*36-5T>C
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ

18-32446088-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32446088
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32446088
    reference: chr 18
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.789+2062A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1496A>G
  hgvsp: ENSP00000382072.5:p.Lys499Arg
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.606+2062A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1505A>G
  hgvsp: ENSP00000472031.1:p.Lys502Arg
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1662+2062A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1662+2062A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.542A>G
  hgvsp: ENSP00000471783.1:p.Lys181Arg
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1496A>G
  hgvsp: ENSP00000473119.1:p.Lys499Arg
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1482+2062A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1676A>G
  hgvsp: ENSP00000269191.6:p.Lys559Arg
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.926A>G
  hgvsp: ENSP00000469121.1:p.Lys309Arg
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1482+2062A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.*49A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1665+2062A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1667A>G
  hgvsp: ENSP00000336682.4:p.Lys556Arg
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1491+2062A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.618+2062A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.528+2062A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.606+2062A>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1491+2062A>G
  variant of: http://identifiers.org/hgnc/3057
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Lys502Arg
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

18-32446093-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32446093
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32446093
    reference: chr 18
allele count: 2
allele frequency: 1.647500741375333e-5
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1665+2067G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1662+2067G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1482+2067G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.789+2067G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.528+2067G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1491+2067G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1482+2067G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1501G>A
  hgvsp: ENSP00000473119.1:p.Gly501Arg
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.547G>A
  hgvsp: ENSP00000471783.1:p.Gly183Arg
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.*54G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1491+2067G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1672G>A
  hgvsp: ENSP00000336682.4:p.Gly558Arg
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.931G>A
  hgvsp: ENSP00000469121.1:p.Gly311Arg
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.606+2067G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1681G>A
  hgvsp: ENSP00000269191.6:p.Gly561Arg
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.618+2067G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1662+2067G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1510G>A
  hgvsp: ENSP00000472031.1:p.Gly504Arg
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.606+2067G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1501G>A
  hgvsp: ENSP00000382072.5:p.Gly501Arg
  variant of: http://identifiers.org/hgnc/3057
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gly504Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

18-32446113-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32446113
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32446113
    reference: chr 18
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1662+2087C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1482+2087C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1665+2087C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.1521C>T
  hgvsp: ENST00000597599.1:c.1521C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.1530C>T
  hgvsp: ENST00000598774.1:c.1530C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.789+2087C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.528+2087C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.1692C>T
  hgvsp: ENST00000348997.5:c.1692C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.606+2087C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470934
  ensembl transcript: ENST00000599844
  gene symbol: DTNA
  hgvsc: ENST00000599844.1:c.*74C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1491+2087C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1662+2087C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1503+18C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.618+2087C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.567C>T
  hgvsp: ENST00000597674.1:c.567C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.606+2087C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1491+2087C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.1701C>T
  hgvsp: ENST00000269191.6:c.1701C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.951C>T
  hgvsp: ENST00000596745.1:c.951C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1482+2087C>T
  variant of: http://identifiers.org/hgnc/3057
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Tyr510Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS

18-32446126-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32446126
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32446126
    reference: chr 18
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1665+2100C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.606+2100C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.528+2100C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1662+2100C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.*1C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.789+2100C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1482+2100C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.*1C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.*1C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.*1C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.606+2100C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.618+2100C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1491+2100C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1662+2100C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.*1C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1503+31C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.*1C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1482+2100C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1491+2100C>G
  variant of: http://identifiers.org/hgnc/3057
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2868
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum

18-32446128-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32446128
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32446128
    reference: chr 18
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1482+2102A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.*3A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1662+2102A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.528+2102A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1482+2102A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.606+2102A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.*3A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.*3A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1662+2102A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.789+2102A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.606+2102A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.*3A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1665+2102A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1491+2102A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.*3A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.618+2102A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.*3A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1503+33A>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1491+2102A>T
  variant of: http://identifiers.org/hgnc/3057
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14235
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: A
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD

18-32446132-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32446132
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32446132
    reference: chr 18
allele count: 11
allele frequency: 9.063941990771259e-5
allele num: 121360
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.*7G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1482+2106G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.*7G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1662+2106G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1662+2106G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.*7G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1665+2106G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.*7G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.*7G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.618+2106G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1482+2106G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.*7G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.606+2106G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1491+2106G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1491+2106G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1503+37G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.606+2106G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.528+2106G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.789+2106G>A
  variant of: http://identifiers.org/hgnc/3057
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2158
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP

18-32446140-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32446140
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32446140
    reference: chr 18
allele count: 2
allele frequency: 1.64836976230508e-5
allele num: 121332
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1503+45G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.*15G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1491+2114G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.528+2114G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.*15G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.*15G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.*15G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.618+2114G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.606+2114G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.*15G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.*15G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.789+2114G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1491+2114G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1662+2114G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1482+2114G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1662+2114G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1665+2114G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.606+2114G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1482+2114G>A
  variant of: http://identifiers.org/hgnc/3057
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: QD

18-32446142-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32446142
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32446142
    reference: chr 18
allele count: 1
allele frequency: 8.245654540057389e-6
allele num: 121276
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1482+2116C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.*17C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1482+2116C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.528+2116C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1491+2116C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.*17C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.*17C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.*17C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.*17C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1665+2116C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.*17C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1491+2116C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1662+2116C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1503+47C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.606+2116C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.789+2116C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1662+2116C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.618+2116C>G
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.606+2116C>G
  variant of: http://identifiers.org/hgnc/3057
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3816
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14021
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

18-32446146-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32446146
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32446146
    reference: chr 18
allele count: 23
allele frequency: 1.896938506202164e-4
allele num: 121248
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1665+2120C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.606+2120C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1482+2120C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.*21C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.606+2120C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.*21C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.*21C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.*21C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.*21C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.*21C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1491+2120C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1662+2120C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.789+2120C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1503+51C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1482+2120C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1662+2120C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1491+2120C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.618+2120C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.528+2120C>T
  variant of: http://identifiers.org/hgnc/3057
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13840
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD

18-32446147-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32446147
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32446147
    reference: chr 18
allele count: 5
allele frequency: 4.12452774157359e-5
allele num: 121226
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.789+2121G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1482+2121G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.*22G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1662+2121G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.*22G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.606+2121G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1482+2121G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.*22G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.*22G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.*22G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.*22G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1491+2121G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1491+2121G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1662+2121G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1665+2121G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.528+2121G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.618+2121G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1503+52G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.606+2121G>A
  variant of: http://identifiers.org/hgnc/3057
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16572
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

18-32446150-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32446150
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32446150
    reference: chr 18
allele count: 5
allele frequency: 4.126433935792688e-5
allele num: 121170
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.*25C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1662+2124C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.789+2124C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1491+2124C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.*25C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1662+2124C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.*25C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1491+2124C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.618+2124C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1665+2124C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1482+2124C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.*25C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.*25C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.606+2124C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1482+2124C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1503+55C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.*25C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.528+2124C>T
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.606+2124C>T
  variant of: http://identifiers.org/hgnc/3057
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2843
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

18-32446154-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32446154
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32446154
    reference: chr 18
allele count: 399
allele frequency: 3.293818518029323e-3
allele num: 121136
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000467720
  ensembl transcript: ENST00000591182
  gene symbol: DTNA
  hgvsc: ENST00000591182.1:c.606+2128G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000405819
  ensembl transcript: ENST00000444659
  gene symbol: DTNA
  hgvsc: ENST00000444659.1:c.1662+2128G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269192
  ensembl transcript: ENST00000269192
  gene symbol: DTNA
  hgvsc: ENST00000269192.7:c.789+2128G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473119
  ensembl transcript: ENST00000597599
  gene symbol: DTNA
  hgvsc: ENST00000597599.1:c.*29G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470152
  ensembl transcript: ENST00000598334
  gene symbol: DTNA
  hgvsc: ENST00000598334.1:c.1482+2128G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000473078
  ensembl transcript: ENST00000595022
  gene symbol: DTNA
  hgvsc: ENST00000595022.1:c.1482+2128G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470716
  ensembl transcript: ENST00000598142
  gene symbol: DTNA
  hgvsc: ENST00000598142.1:c.1491+2128G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382072
  ensembl transcript: ENST00000399121
  gene symbol: DTNA
  hgvsc: ENST00000399121.5:c.1503+59G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000283365
  ensembl transcript: ENST00000283365
  gene symbol: DTNA
  hgvsc: ENST00000283365.9:c.1491+2128G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382064
  ensembl transcript: ENST00000399113
  gene symbol: DTNA
  hgvsc: ENST00000399113.3:c.1662+2128G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000472031
  ensembl transcript: ENST00000598774
  gene symbol: DTNA
  hgvsc: ENST00000598774.1:c.*29G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269190
  ensembl transcript: ENST00000269190
  gene symbol: DTNA
  hgvsc: ENST00000269190.7:c.1665+2128G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000336682
  ensembl transcript: ENST00000348997
  gene symbol: DTNA
  hgvsc: ENST00000348997.5:c.*29G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000471783
  ensembl transcript: ENST00000597674
  gene symbol: DTNA
  hgvsc: ENST00000597674.1:c.*29G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000469121
  ensembl transcript: ENST00000596745
  gene symbol: DTNA
  hgvsc: ENST00000596745.1:c.*29G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000470247
  ensembl transcript: ENST00000601125
  gene symbol: DTNA
  hgvsc: ENST00000601125.1:c.528+2128G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000382048
  ensembl transcript: ENST00000399097
  gene symbol: DTNA
  hgvsc: ENST00000399097.3:c.606+2128G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000269191
  ensembl transcript: ENST00000269191
  gene symbol: DTNA
  hgvsc: ENST00000269191.6:c.*29G>A
  variant of: http://identifiers.org/hgnc/3057
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134769
  ensembl protein: ENSP00000452255
  ensembl transcript: ENST00000556414
  gene symbol: DTNA
  hgvsc: ENST00000556414.3:c.618+2128G>A
  variant of: http://identifiers.org/hgnc/3057
canonical: false
consequence: 3' UTR
filter: PASS
num of homozygotes: 3
reference allele: G

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000134769
ensembl protein: ENSP00000473078
ensembl transcript: ENST00000595022
gene symbol: DTNA
hgvsc: ENST00000595022.1:c.1336G>C
hgvsp: ENSP00000473078.1:p.Glu446Gln
variant of: http://identifiers.org/hgnc/3057

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000134769
ensembl protein: ENSP00000470934
ensembl transcript: ENST00000599844
gene symbol: DTNA
hgvsc: ENST00000599844.1:c.382G>C
hgvsp: ENSP00000470934.1:p.Glu128Gln
variant of: http://identifiers.org/hgnc/3057

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

GenotypeDepth
all individuals: 323
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 262
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 289
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 285
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 139
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 424
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 501
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2690
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11069
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 371
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 225
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 442
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 38802
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 465
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 232
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 718
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2907
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 235
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 899
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 587
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6808
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 452
bin: 2.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 58
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3724
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 946
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46370
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10266
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506614035616356e-5
allele num: 66374
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16438
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.53e-1

QD
type: SiteQuality
SIO_000300: 1.029e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.7e-2

MQRankSum
type: SiteQuality
SIO_000300: -2.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.92e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.19e0

DP
type: SiteQuality
SIO_000300: 1.849447e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.47e-1

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000134769
ensembl protein: ENSP00000283365
ensembl transcript: ENST00000283365
gene symbol: DTNA
hgvsc: ENST00000283365.9:c.1346A>T
hgvsp: ENSP00000283365.9:p.Glu449Val
variant of: http://identifiers.org/hgnc/3057

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000134769
ensembl protein: ENSP00000471783
ensembl transcript: ENST00000597674
gene symbol: DTNA
hgvsc: ENST00000597674.1:c.383A>T
hgvsp: ENSP00000471783.1:p.Glu128Val
variant of: http://identifiers.org/hgnc/3057

GenotypeDepth
all individuals: 263
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 422
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 465
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 137
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 225
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 331
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 38796
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 289
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 285
bin: 4.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 718
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 236
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 11076
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2683
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2907
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 232
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 442
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 501
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 371
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3731
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46346
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 46
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 463
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 589
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 64
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 902
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6808
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 290
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 948
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.083465141744738e-5
allele num: 16438
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10264
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66374
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.822e0

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

DP
type: SiteQuality
SIO_000300: 1.849298e6

QD
type: SiteQuality
SIO_000300: 1.421e1

MQ
type: SiteQuality
SIO_000300: 5.966e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.03e0

VQSLOD
type: SiteQuality
SIO_000300: 5.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.95e-1

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000134769
ensembl protein: ENSP00000470247
ensembl transcript: ENST00000601125
gene symbol: DTNA
hgvsc: ENST00000601125.1:c.388G>A
hgvsp: ENSP00000470247.1:p.Ala130Thr
variant of: http://identifiers.org/hgnc/3057

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000134769
ensembl protein: ENSP00000283365
ensembl transcript: ENST00000283365
gene symbol: DTNA
hgvsc: ENST00000283365.9:c.1351G>A
hgvsp: ENSP00000283365.9:p.Ala451Thr
variant of: http://identifiers.org/hgnc/3057

GenotypeDepth
all individuals: 337
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 501
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 38772
bin: 2.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 465
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2683
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 423
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 128
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 277
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 235
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 720
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 232
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 371
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 289
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 285
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 442
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2908
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 11086
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 225
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46342
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 947
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 73
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 6808
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3719
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 903
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 3.75e1
variant carriers: 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: 10260
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16436
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.14e-1

MQ
type: SiteQuality
SIO_000300: 5.981e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.41e0

FS
type: SiteQuality
SIO_000300: 3.738e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.061e0

VQSLOD
type: SiteQuality
SIO_000300: -6.025e-1

QD
type: SiteQuality
SIO_000300: 8.550000000000001e0

DP
type: SiteQuality
SIO_000300: 1.84925e6

MQRankSum
type: SiteQuality
SIO_000300: -2.07e-1

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000134769
ensembl protein: ENSP00000283365
ensembl transcript: ENST00000283365
gene symbol: DTNA
hgvsc: ENST00000283365.9:c.1361A>G
hgvsp: ENSP00000283365.9:p.Asn454Ser
variant of: http://identifiers.org/hgnc/3057

GenotypeDepth
all individuals: 232
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 38636
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 286
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 371
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 718
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 289
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 386
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2697
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 465
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 235
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 341
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2907
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11104
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 225
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 423
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 501
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 442
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 74
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 578
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 945
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6807
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3717
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46224
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 891
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10238
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508113651444773e-5
allele num: 66308
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16428
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 8.407999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: 3.6e-1

DP
type: SiteQuality
SIO_000300: 1.848066e6

MQ
type: SiteQuality
SIO_000300: 5.968e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

QD
type: SiteQuality
SIO_000300: 1.016e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.66e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.5e-2

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000134769
ensembl protein: ENSP00000470247
ensembl transcript: ENST00000601125
gene symbol: DTNA
hgvsc: ENST00000601125.1:c.402C>A
hgvsp: ENST00000601125.1:c.402C>A(p.%3D)
variant of: http://identifiers.org/hgnc/3057

GenotypeDepth
all individuals: 235
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 423
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 288
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 721
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 122
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 410
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 501
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2681
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 371
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 465
bin: 8.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 11127
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 442
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 391
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 225
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 289
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 38549
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2907
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 232
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 642
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46200
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 69
bin: 5.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 79
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6808
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 64
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 578
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3707
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 887
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 939
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16424
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10234
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508750754375377e-5
allele num: 66280
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 5.85e-1

MQ
type: SiteQuality
SIO_000300: 5.994e1

MQRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.849e0

DP
type: SiteQuality
SIO_000300: 1.847318e6

QD
type: SiteQuality
SIO_000300: 8.16e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.27e-1

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000134769
ensembl protein: ENSP00000283365
ensembl transcript: ENST00000283365
gene symbol: DTNA
hgvsc: ENST00000283365.9:c.1365C>G
hgvsp: ENST00000283365.9:c.1365C>G(p.%3D)
variant of: http://identifiers.org/hgnc/3057

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

GenotypeDepth
all individuals: 289
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 501
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11127
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 288
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 423
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 721
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 410
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 371
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 391
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 38549
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 232
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2681
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 122
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 465
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 235
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 225
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2907
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 442
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 887
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 939
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 88
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 69
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3707
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 578
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 642
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6808
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 46200
bin: 6.25e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16424
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66280
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10234
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.849e0

QD
type: SiteQuality
SIO_000300: 8.16e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.85e-1

DP
type: SiteQuality
SIO_000300: 1.847318e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.994e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 6.26e-1

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000134769
ensembl protein: ENSP00000470247
ensembl transcript: ENST00000601125
gene symbol: DTNA
hgvsc: ENST00000601125.1:c.404C>T
hgvsp: ENSP00000470247.1:p.Thr135Ile
variant of: http://identifiers.org/hgnc/3057

GenotypeDepth
all individuals: 2907
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 371
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 125
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 726
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 501
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 235
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 417
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 433
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 11143
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 424
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 232
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 465
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 285
bin: 4.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 442
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2685
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 225
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 289
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 38474
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 932
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 291
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3697
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 46162
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 45
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 68
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6806
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 577
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 883
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 679
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509388395822013e-5
allele num: 66252
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16418
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10230
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.035e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.186e0

QD
type: SiteQuality
SIO_000300: 1.217e1

DP
type: SiteQuality
SIO_000300: 1.846953e6

VQSLOD
type: SiteQuality
SIO_000300: 8.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.08e0

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000134769
ensembl protein: ENSP00000472031
ensembl transcript: ENST00000598774
gene symbol: DTNA
hgvsc: ENST00000598774.1:c.1384C>T
hgvsp: ENSP00000472031.1:p.Arg462Trp
variant of: http://identifiers.org/hgnc/3057

GenotypeDepth
all individuals: 2692
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11099
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 289
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 698
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 442
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 226
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 288
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 37620
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 233
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 423
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 926
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 235
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 371
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 233
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 501
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 465
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 720
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2907
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 53
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 3597
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 568
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 854
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 910
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45288
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1253
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6804
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 119
bin: 5.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.114711997064938e-5
allele num: 16354
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65966
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11446
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10106
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.88e0

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.51e0

MQRankSum
type: SiteQuality
SIO_000300: 9.389999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.41e-1

DP
type: SiteQuality
SIO_000300: 1.83749e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.98e1

FS
type: SiteQuality
SIO_000300: 1.725e0

QD
type: SiteQuality
SIO_000300: 1.027e1

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000134769
ensembl protein: ENSP00000472031
ensembl transcript: ENST00000598774
gene symbol: DTNA
hgvsc: ENST00000598774.1:c.1386G>A
hgvsp: ENST00000598774.1:c.1386G>A(p.%3D)
variant of: http://identifiers.org/hgnc/3057

GenotypeDepth
all individuals: 37484
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 11069
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 225
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2680
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 250
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 232
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 236
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1039
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 422
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2906
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 502
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 287
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 744
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 723
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 465
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 371
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 289
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 442
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 73
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 565
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 904
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45133
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3584
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6805
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 44
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1367
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 849
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11436
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16340
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65928
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10080
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.164144353899884e-4
allele num: 8590
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.835254e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.63e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.953e1

VQSLOD
type: SiteQuality
SIO_000300: 4.52e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.053e0

FS
type: SiteQuality
SIO_000300: 9.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.54e-1

QD
type: SiteQuality
SIO_000300: 8.66e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000134769
ensembl protein: ENSP00000470934
ensembl transcript: ENST00000599844
gene symbol: DTNA
hgvsc: ENST00000599844.1:c.424C>T
hgvsp: ENSP00000470934.1:p.Leu142Phe
variant of: http://identifiers.org/hgnc/3057

GenotypeDepth
all individuals: 253
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 442
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11096
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1103
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 289
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 235
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 769
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 501
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 420
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 286
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 225
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2656
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 371
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 721
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 232
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 465
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 37393
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2907
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 1441
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45049
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 565
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 24
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3578
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 904
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 847
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 225
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6804
bin: 9.75e1
variant carriers: 1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.120700208103807e-5
allele num: 16338
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65908
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.34e0

VQSLOD
type: SiteQuality
SIO_000300: -9.205e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 8.43e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.329e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.17e-1

MQ
type: SiteQuality
SIO_000300: 5.958e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.58e-1

DP
type: SiteQuality
SIO_000300: 1.834016e6

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000134769
ensembl protein: ENSP00000382072
ensembl transcript: ENST00000399121
gene symbol: DTNA
hgvsc: ENST00000399121.5:c.1385+4G>A
variant of: http://identifiers.org/hgnc/3057

GenotypeDepth
all individuals: 425
bin: 4.25e1
variant carriers: 2

GenotypeDepth
all individuals: 371
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 35780
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 559
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 727
bin: 3.75e1
variant carriers: 2

GenotypeDepth
all individuals: 41
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 501
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 287
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 289
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2907
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 232
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2661
bin: 3.25e1
variant carriers: 3

GenotypeDepth
all individuals: 1143
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 10810
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 238
bin: 5.25e1
variant carriers: 3

GenotypeDepth
all individuals: 465
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2282
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 226
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 442
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6815
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 101
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 533
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2485
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3473
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 590
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 822
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 551
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 878
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 43181
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11338
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16230
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9952
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 1.833012556136009e-4
allele num: 65466
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
type: SiteQuality
SIO_000300: 4.062e0

MQ
type: SiteQuality
SIO_000300: 5.953e1

MQRankSum
type: SiteQuality
SIO_000300: -5.0e-2

QD
type: SiteQuality
SIO_000300: 1.388e1

VQSLOD
type: SiteQuality
SIO_000300: 7.87e-1

DP
type: SiteQuality
SIO_000300: 1.814346e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.24e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.75e-1

GenotypeDepth
all individuals: 70
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 371
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4055
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 728
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1510
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 33524
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 225
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10365
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 285
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 232
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1134
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 420
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 235
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 289
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 465
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2628
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2907
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 442
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3784
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6801
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 240
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 849
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40414
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 798
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 978
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3324
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 537
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 607
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1150
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16152
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.888888888888889e-5
allele num: 11250
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6528
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9862
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64944
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8532
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e0

VQSLOD
type: SiteQuality
SIO_000300: 1.58e-1

QD
type: SiteQuality
SIO_000300: 1.437e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -7.29e-1

MQ
type: SiteQuality
SIO_000300: 5.936e1

MQRankSum
type: SiteQuality
SIO_000300: 5.39e-1

FS
type: SiteQuality
SIO_000300: 6.658e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.141e0

DP
type: SiteQuality
SIO_000300: 1.785783e6

GenotypeDepth
all individuals: 124
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 371
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9818
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2908
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 422
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 235
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 465
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 289
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2448
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 232
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 724
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29389
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 442
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1976
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 291
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2580
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 501
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 225
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1286
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 381
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2917
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 526
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5621
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 409
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 741
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1780
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35589
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 466
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2211
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6803
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 219
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 822
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.107906514172053e-5
allele num: 64352
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11178
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8434
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6496
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16058
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.8153e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.26e0

DP
type: SiteQuality
SIO_000300: 1.741564e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.615e0

MQRankSum
type: SiteQuality
SIO_000300: 7.15e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.23e-1

QD
type: SiteQuality
SIO_000300: 1.304e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.99e-1

GenotypeDepth
all individuals: 29389
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2580
bin: 3.25e1
variant carriers: 2

GenotypeDepth
all individuals: 9818
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6946
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 422
bin: 4.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 225
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1976
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 124
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2448
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 371
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 289
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2908
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 724
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 501
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 235
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 465
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 232
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 409
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2917
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1780
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 466
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 526
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1286
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35589
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 822
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6803
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 381
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5621
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2211
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 741
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.107906514172053e-5
allele num: 64352
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16058
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6496
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8434
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11178
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.99e-1

FS
type: SiteQuality
SIO_000300: 1.8153e1

VQSLOD
type: SiteQuality
SIO_000300: -1.615e0

MQRankSum
type: SiteQuality
SIO_000300: 7.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.23e-1

DP
type: SiteQuality
SIO_000300: 1.741564e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.26e0

QD
type: SiteQuality
SIO_000300: 1.304e1

GenotypeDepth
all individuals: 320
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12127
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 234
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16282
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2907
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13437
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 442
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 283
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 373
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 414
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 664
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 233
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 225
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 290
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 501
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1804
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6434
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 466
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 371
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2379
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 776
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3768
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6437
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 546
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2087
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6798
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 756
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5855
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7847
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2279
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 520
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18361
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10952
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.591748376416656e-5
allele num: 62824
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6420
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9394
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8192
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15842
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.895e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.35e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.020999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.793e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.002e0

QD
type: SiteQuality
SIO_000300: 1.079e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

DP
type: SiteQuality
SIO_000300: 1.598941e6

GenotypeDepth
all individuals: 26088
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1500
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10964
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 798
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 493
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 239
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 285
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 522
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9796
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 438
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 404
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2839
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 493
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 645
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 614
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1085
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 528
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1364
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 876
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4033
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2563
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 611
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1875
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6539
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4970
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 450
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14185
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 890
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 839
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9195
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 507
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 768
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1054
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4893
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5934
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9970
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3390
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4990
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4290
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.213719871902916e-5
allele num: 23732
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2166
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 408
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 9.28606e5

QD
type: SiteQuality
SIO_000300: 1.48e1

VQSLOD
type: SiteQuality
SIO_000300: 3.87e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.56e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.532e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.64e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.75e0

GenotypeDepth
all individuals: 1509
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4026
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 522
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 438
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 493
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 404
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 880
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6204
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 10917
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 528
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 647
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1540
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 493
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28447
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 510
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 798
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 614
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 285
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 239
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 845
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5937
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4139
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2091
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24958
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4788
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 602
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2220
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4412
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2231
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 473
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5296
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 506
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 450
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5208
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 434
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.756339581036384e-4
allele num: 3628
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10162
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2356
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.98406374501992e-5
allele num: 25100
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4624
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.08e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.63e0

MQRankSum
type: SiteQuality
SIO_000300: 2.59e-1

FS
type: SiteQuality
SIO_000300: 6.875e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.59e0

QD
type: SiteQuality
SIO_000300: 1.361e1

DP
type: SiteQuality
SIO_000300: 9.84477e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 1572
bin: 2.75e1
variant carriers: 4

GenotypeDepth
all individuals: 438
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 283
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 238
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10855
bin: 1.25e1
variant carriers: 14

GenotypeDepth
all individuals: 28534
bin: 7.5e0
variant carriers: 12

GenotypeDepth
all individuals: 493
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 881
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 510
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1124
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 648
bin: 4.75e1
variant carriers: 2

GenotypeDepth
all individuals: 797
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 522
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5956
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 618
bin: 9.75e1
variant carriers: 6

GenotypeDepth
all individuals: 1484
bin: 1.75e1
variant carriers: 8

GenotypeDepth
all individuals: 530
bin: 5.75e1
variant carriers: 2

GenotypeDepth
all individuals: 404
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 492
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 583
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 8.75e1
variant carriers: 3

GenotypeQuality
all individuals: 378
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4109
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1946
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4723
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5126
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25424
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 445
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 842
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1925
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4726
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 383
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2152
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 506
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 451
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 5975
bin: 9.75e1
variant carriers: 47

GenotypeQuality
all individuals: 388
bin: 8.25e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3626
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10162
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2354
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 428
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 4.32152117545376e-4
allele num: 4628
num of homozygotes: 0

African
type: Population
allele count: 39
allele frequency: 7.422915873620099e-3
allele num: 5254
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.969829297340214e-5
allele num: 25190
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.62e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.02e0

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

DP
type: SiteQuality
SIO_000300: 9.89662e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.5e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.6e-1

QD
type: SiteQuality
SIO_000300: 1.422e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.14e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.35e-1

GenotypeDepth
all individuals: 438
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1647
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 648
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 521
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 529
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 28553
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 615
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 493
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1583
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1142
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5351
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 510
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 404
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 879
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 492
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 797
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4777
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 283
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 239
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1694
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2075
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4015
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5232
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1718
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 863
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4717
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 478
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 510
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 391
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25893
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 587
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 389
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4585
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5931
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 449
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4750
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 7.800920508620017e-5
allele num: 25638
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5238
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3670
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10230
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2418
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 440
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.04e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.52e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.81e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

QD
type: SiteQuality
SIO_000300: 1.277e1

DP
type: SiteQuality
SIO_000300: 1.003104e6

FS
type: SiteQuality
SIO_000300: 6.96e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.27e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 10707
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 404
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 615
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 493
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28553
bin: 7.5e0
variant carriers: 2

GenotypeDepth
all individuals: 1142
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1583
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4777
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 438
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5351
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 510
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 492
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 239
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 879
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 797
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 648
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 529
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 283
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 521
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4585
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2075
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 510
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 391
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 136
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1718
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 478
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25893
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1694
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5232
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4717
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 863
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 587
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4015
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5931
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 211
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 449
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10230
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4750
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2418
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3670
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5238
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 1.560184101724003e-4
allele num: 25638
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 440
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

DP
type: SiteQuality
SIO_000300: 1.003104e6

FS
type: SiteQuality
SIO_000300: 6.96e-1

QD
type: SiteQuality
SIO_000300: 1.277e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.52e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.04e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.81e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.27e0

GenotypeDepth
all individuals: 649
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2979
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 28764
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 1878
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9033
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 239
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 614
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1352
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 493
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8643
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 511
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 529
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 284
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1175
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 438
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 879
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 492
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 522
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 404
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27832
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9194
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1653
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5943
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3743
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 786
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 999
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 689
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3573
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 390
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2808
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 452
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5632
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 462
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5520
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10550
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2708
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4230
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28326
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.5e-1

FS
type: SiteQuality
SIO_000300: 3.68e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.6e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

DP
type: SiteQuality
SIO_000300: 1.065052e6

GenotypeDepth
all individuals: 1187
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 511
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 492
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 284
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 881
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 799
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 438
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1347
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 493
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28424
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 9611
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8647
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2672
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1940
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 239
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 404
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 614
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 529
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 522
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 417
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 536
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 391
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1572
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1023
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3423
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5943
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 639
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 744
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 419
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27657
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2541
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3543
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 452
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10040
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5708
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4332
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2794
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 478
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.458532198934772e-5
allele num: 28914
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10622
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5690
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.079789e6

MQRankSum
type: SiteQuality
SIO_000300: -5.75e-1

MQ
type: SiteQuality
SIO_000300: 5.913e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.259e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.507e0

FS
type: SiteQuality
SIO_000300: 1.672e0

QD
type: SiteQuality
SIO_000300: 1.497e1

VQSLOD
type: SiteQuality
SIO_000300: -5.87e-2

GenotypeDepth
all individuals: 438
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 649
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14185
bin: 2.25e1
variant carriers: 2

GenotypeDepth
all individuals: 239
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 511
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 529
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1553
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 879
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1392
bin: 1.75e1
variant carriers: 12

GenotypeDepth
all individuals: 2346
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 404
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26031
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 799
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1236
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 522
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 284
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 492
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 614
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 493
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 557
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2795
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1207
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 353
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2754
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14488
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 501
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25848
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1303
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1507
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 452
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5960
bin: 9.75e1
variant carriers: 18

GenotypeQuality
all individuals: 567
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 444
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6894
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 2.134927412467976e-4
allele num: 32788
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11098
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 13
allele frequency: 4.0e-3
allele num: 3250
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6162
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.915708812260536e-3
allele num: 522
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5102
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.151987e6

VQSLOD
type: SiteQuality
SIO_000300: 4.37e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -7.15e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -3.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.5e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.87e-1

QD
type: SiteQuality
SIO_000300: 1.337e1

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000134769
ensembl protein: ENSP00000473078
ensembl transcript: ENST00000595022
gene symbol: DTNA
hgvsc: ENST00000595022.1:c.1391G>A
hgvsp: ENSP00000473078.1:p.Arg464His
variant of: http://identifiers.org/hgnc/3057

GenotypeDepth
all individuals: 4592
bin: 1.25e1
variant carriers: 4

GenotypeDepth
all individuals: 511
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3570
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 649
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 594
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 521
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1451
bin: 3.25e1
variant carriers: 4

GenotypeDepth
all individuals: 1565
bin: 1.75e1
variant carriers: 3

GenotypeDepth
all individuals: 529
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 23031
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 19028
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 239
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 438
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 615
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 284
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 404
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 493
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 802
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 492
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 894
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1564
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22946
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1758
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 692
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 201
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 783
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1656
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 581
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 898
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 518
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 428
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 411
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 605
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 19434
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 918
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5954
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 459
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 4.73260766682442e-4
allele num: 4226
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6620
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8744
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12226
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7226
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 2.890173410404624e-4
allele num: 41520
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.12e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.47e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.22e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e-1

DP
type: SiteQuality
SIO_000300: 1.301467e6

QD
type: SiteQuality
SIO_000300: 1.13e1

FS
type: SiteQuality
SIO_000300: 2.032e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000134769
ensembl protein: ENSP00000382048
ensembl transcript: ENST00000399097
gene symbol: DTNA
hgvsc: ENST00000399097.3:c.522T>C
hgvsp: ENST00000399097.3:c.522T>C(p.%3D)
variant of: http://identifiers.org/hgnc/3057

GenotypeDepth
all individuals: 493
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 649
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 511
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 239
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 408
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 438
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3714
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1228
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 800
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16087
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 889
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1375
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 492
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 285
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 521
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 27081
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 529
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3947
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 614
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 404
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 554
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 449
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 681
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1228
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1351
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28283
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1773
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16696
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5947
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 461
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12808
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 672
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9266
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.175331738090059e-5
allele num: 45970
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7212
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4684
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7676
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.03e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.74e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.68e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.74e-1

DP
type: SiteQuality
SIO_000300: 1.356974e6

MQRankSum
type: SiteQuality
SIO_000300: 2.03e0

VQSLOD
type: SiteQuality
SIO_000300: -9.409999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000134769
ensembl protein: ENSP00000469121
ensembl transcript: ENST00000596745
gene symbol: DTNA
hgvsc: ENST00000596745.1:c.840G>C
hgvsp: ENSP00000469121.1:p.Gln280His
variant of: http://identifiers.org/hgnc/3057

GenotypeDepth
all individuals: 529
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 649
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1501
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12968
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4904
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 511
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 239
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1384
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 801
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 521
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 893
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 614
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3201
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 274
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 493
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 285
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29602
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 404
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 492
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 438
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1113
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 606
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1083
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 585
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1017
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1881
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13816
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 832
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30443
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 585
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 450
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5949
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 686
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7660
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.99896054051893e-5
allele num: 50026
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8136
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5074
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13342
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 714
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9766
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.575e0

MQRankSum
type: SiteQuality
SIO_000300: -2.41e-1

DP
type: SiteQuality
SIO_000300: 1.416083e6

FS
type: SiteQuality
SIO_000300: 9.47e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.25e-1

MQ
type: SiteQuality
SIO_000300: 5.895e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.900000000000001e-2

QD
type: SiteQuality
SIO_000300: 6.42e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.44e-1

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000134769
ensembl protein: ENSP00000283365
ensembl transcript: ENST00000283365
gene symbol: DTNA
hgvsc: ENST00000283365.9:c.1443C>T
hgvsp: ENST00000283365.9:c.1443C>T(p.%3D)
variant of: http://identifiers.org/hgnc/3057

GenotypeDepth
all individuals: 404
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10847
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 529
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 521
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1608
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 900
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5981
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1643
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 239
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 224
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 614
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 648
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 29467
bin: 2.25e1
variant carriers: 2

GenotypeDepth
all individuals: 805
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 492
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 511
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 285
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 438
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 493
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4053
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1116
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12859
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 31430
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 596
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 365
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1904
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 666
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5949
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 456
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1175
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 735
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1013
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 676
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 5.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 734
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13674
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7902
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.689576695493855e-5
allele num: 52728
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5344
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10066
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.449246e6

VQSLOD
type: SiteQuality
SIO_000300: 5.88e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

QD
type: SiteQuality
SIO_000300: 1.463e1

MQ
type: SiteQuality
SIO_000300: 5.922e1

FS
type: SiteQuality
SIO_000300: 8.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.16e-1

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000134769
ensembl protein: ENSP00000283365
ensembl transcript: ENST00000283365
gene symbol: DTNA
hgvsc: ENST00000283365.9:c.1449A>G
hgvsp: ENST00000283365.9:c.1449A>G(p.%3D)
variant of: http://identifiers.org/hgnc/3057

GenotypeDepth
all individuals: 4734
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 511
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 493
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 246
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 28887
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 492
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 521
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 239
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10840
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 801
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6020
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 438
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 285
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 892
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 404
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1533
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1576
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 529
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 614
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 647
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1901
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 685
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 641
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5949
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 446
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13468
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1157
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31742
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 669
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 445
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1032
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8458
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10052
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5350
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52928
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.267748478701826e-4
allele num: 7888
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13702
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 736
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -9.83e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.2e-1

DP
type: SiteQuality
SIO_000300: 1.441995e6

VQSLOD
type: SiteQuality
SIO_000300: -3.274e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.94e-1

QD
type: SiteQuality
SIO_000300: 2.63e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

MQ
type: SiteQuality
SIO_000300: 5.855e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.36e-1

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000134769
ensembl protein: ENSP00000473078
ensembl transcript: ENST00000595022
gene symbol: DTNA
hgvsc: ENST00000595022.1:c.1477C>T
hgvsp: ENST00000595022.1:c.1477C>T(p.%3D)
variant of: http://identifiers.org/hgnc/3057

GenotypeDepth
all individuals: 1355
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12972
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 801
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1239
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4251
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 491
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14218
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5776
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 404
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14012
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 521
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 285
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 531
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 647
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 511
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 238
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 615
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 438
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 884
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 493
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1171
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 603
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2439
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15114
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 458
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3131
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22143
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5946
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 263
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 460
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 535
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1412
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3930
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48356
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 676
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.682851874615857e-5
allele num: 13016
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8826
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6444
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8108
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4990
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.365e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.78e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.34e-1

MQ
type: SiteQuality
SIO_000300: 5.978e1

FS
type: SiteQuality
SIO_000300: 7.129e0

QD
type: SiteQuality
SIO_000300: 1.051e1

MQRankSum
type: SiteQuality
SIO_000300: -3.0e-2

DP
type: SiteQuality
SIO_000300: 1.254718e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.0e-1

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000134769
ensembl protein: ENSP00000283365
ensembl transcript: ENST00000283365
gene symbol: DTNA
hgvsc: ENST00000283365.9:c.1488A>G
hgvsp: ENST00000283365.9:c.1488A>G(p.%3D)
variant of: http://identifiers.org/hgnc/3057

GenotypeDepth
all individuals: 492
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 521
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 531
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 438
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 801
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 647
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12051
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 882
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 285
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1335
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1363
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4052
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14219
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 511
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6218
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 614
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 404
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 238
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14582
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 493
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1553
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 536
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4093
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14210
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22540
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3220
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2598
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 777
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1161
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 524
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5948
bin: 9.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48132
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8076
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6352
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4946
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 676
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.300437083045779e-4
allele num: 8694
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12940
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.56e-1

DP
type: SiteQuality
SIO_000300: 1.242149e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.18e0

FS
type: SiteQuality
SIO_000300: 6.283e0

MQRankSum
type: SiteQuality
SIO_000300: 7.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 9.21e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.32e1

GenotypeDepth
all individuals: 2447
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 878
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2704
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7429
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 491
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16276
bin: 1.25e1
variant carriers: 2

GenotypeDepth
all individuals: 801
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1245
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 531
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 614
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7694
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 438
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 493
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 511
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1348
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5950
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2946
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22907
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1179
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 528
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3709
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 898
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4735
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3467
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2026
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 884
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6468
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1693
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 411
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5526
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7756
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 644
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4674
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12456
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.734006734006734e-5
allele num: 44550
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7704
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.4e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -8.67e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e-1

MQ
type: SiteQuality
SIO_000300: 5.604e1

DP
type: SiteQuality
SIO_000300: 1.164188e6

VQSLOD
type: SiteQuality
SIO_000300: 1.89e0

QD
type: SiteQuality
SIO_000300: 2.97e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.24e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-1

GenotypeDepth
all individuals: 438
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15968
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 801
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 238
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 521
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7694
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1245
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7429
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 878
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2704
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 404
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16276
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 531
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 646
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2447
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 491
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 511
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 614
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 493
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1693
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 898
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2946
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6468
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1179
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4735
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22907
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2026
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3467
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 884
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5950
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3709
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1348
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 528
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 411
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4674
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44550
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.809627216793341e-4
allele num: 5526
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7704
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7756
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12456
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 644
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.97e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.4e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.164188e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.24e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.89e0

MQ
type: SiteQuality
SIO_000300: 5.604e1

GenotypeDepth
all individuals: 438
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 800
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 492
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 521
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7229
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 510
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 404
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2706
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 493
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 646
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16176
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 16671
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 531
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6662
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3006
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1272
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 614
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 285
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 880
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3746
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1307
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1791
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1241
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 409
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4731
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3465
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4795
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22175
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2949
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3484
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1339
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 531
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 411
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 874
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5948
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4568
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7470
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7554
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 640
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43168
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12292
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.910584638899503e-4
allele num: 5234
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.464e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.453e0

DP
type: SiteQuality
SIO_000300: 1.147366e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.768e0

QD
type: SiteQuality
SIO_000300: 5.41e0

Annotation
canonical: false
clinical significance: benign
consequence: intron_variant
ensembl gene: ENSG00000134769
ensembl protein: ENSP00000269192
ensembl transcript: ENST00000269192
gene symbol: DTNA
hgvsc: ENST00000269192.7:c.789+14G>A
variant of: http://identifiers.org/hgnc/3057

GenotypeDepth
all individuals: 2558
bin: 2.75e1
variant carriers: 1323

GenotypeDepth
all individuals: 490
bin: 5.75e1
variant carriers: 344

GenotypeDepth
all individuals: 1012
bin: 3.75e1
variant carriers: 317

GenotypeDepth
all individuals: 220
bin: 9.25e1
variant carriers: 168

GenotypeDepth
all individuals: 487
bin: 6.25e1
variant carriers: 373

GenotypeDepth
all individuals: 859
bin: 4.25e1
variant carriers: 269

GenotypeDepth
all individuals: 3046
bin: 2.5e0
variant carriers: 192

GenotypeDepth
all individuals: 15222
bin: 7.5e0
variant carriers: 3984

GenotypeDepth
all individuals: 5161
bin: 2.25e1
variant carriers: 3090

GenotypeDepth
all individuals: 1573
bin: 9.75e1
variant carriers: 1385

GenotypeDepth
all individuals: 17797
bin: 1.25e1
variant carriers: 8307

GenotypeDepth
all individuals: 1384
bin: 3.25e1
variant carriers: 585

GenotypeDepth
all individuals: 512
bin: 6.75e1
variant carriers: 421

GenotypeDepth
all individuals: 246
bin: 8.75e1
variant carriers: 205

GenotypeDepth
all individuals: 398
bin: 7.75e1
variant carriers: 340

GenotypeDepth
all individuals: 7487
bin: 1.75e1
variant carriers: 6359

GenotypeDepth
all individuals: 427
bin: 7.25e1
variant carriers: 369

GenotypeDepth
all individuals: 690
bin: 4.75e1
variant carriers: 283

GenotypeDepth
all individuals: 350
bin: 8.25e1
variant carriers: 280

GenotypeDepth
all individuals: 574
bin: 5.25e1
variant carriers: 335

GenotypeQuality
all individuals: 466
bin: 4.25e1
variant carriers: 392

GenotypeQuality
all individuals: 961
bin: 9.25e1
variant carriers: 642

GenotypeQuality
all individuals: 727
bin: 8.25e1
variant carriers: 449

GenotypeQuality
all individuals: 712
bin: 4.75e1
variant carriers: 639

GenotypeQuality
all individuals: 1772
bin: 3.25e1
variant carriers: 761

GenotypeQuality
all individuals: 16659
bin: 2.25e1
variant carriers: 614

GenotypeQuality
all individuals: 1023
bin: 1.75e1
variant carriers: 399

GenotypeQuality
all individuals: 849
bin: 6.75e1
variant carriers: 377

GenotypeQuality
all individuals: 710
bin: 8.75e1
variant carriers: 530

GenotypeQuality
all individuals: 1785
bin: 2.75e1
variant carriers: 419

GenotypeQuality
all individuals: 768
bin: 1.25e1
variant carriers: 214

GenotypeQuality
all individuals: 493
bin: 5.75e1
variant carriers: 412

GenotypeQuality
all individuals: 1111
bin: 3.75e1
variant carriers: 715

GenotypeQuality
all individuals: 3057
bin: 7.5e0
variant carriers: 164

GenotypeQuality
all individuals: 1934
bin: 2.5e0
variant carriers: 103

GenotypeQuality
all individuals: 491
bin: 7.25e1
variant carriers: 288

GenotypeQuality
all individuals: 22214
bin: 9.75e1
variant carriers: 20270

GenotypeQuality
all individuals: 672
bin: 5.25e1
variant carriers: 592

GenotypeQuality
all individuals: 733
bin: 7.75e1
variant carriers: 395

GenotypeQuality
all individuals: 3356
bin: 6.25e1
variant carriers: 554

East Asian
type: Population
allele count: 333
allele frequency: 6.524294670846395e-2
allele num: 5104
num of homozygotes: 6

South Asian
type: Population
allele count: 3788
allele frequency: 3.031855290539459e-1
allele num: 12494
num of homozygotes: 531

Latino
type: Population
allele count: 1488
allele frequency: 2.022838499184339e-1
allele num: 7356
num of homozygotes: 126

African
type: Population
allele count: 4182
allele frequency: 5.401704985791785e-1
allele num: 7742
num of homozygotes: 1040

European (Non-Finnish)
type: Population
allele count: 17189
allele frequency: 3.94405947409481e-1
allele num: 43582
num of homozygotes: 2758

European (Finnish)
type: Population
allele count: 2012
allele frequency: 4.341821320673284e-1
allele num: 4634
num of homozygotes: 336

Other
type: Population
allele count: 252
allele frequency: 3.9375e-1
allele num: 640
num of homozygotes: 47

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.96e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.54e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.67e-2

DP
type: SiteQuality
SIO_000300: 1.282942e6

MQRankSum
type: SiteQuality
SIO_000300: 6.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.73e-1

QD
type: SiteQuality
SIO_000300: 1.793e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.007e0

GenotypeDepth
all individuals: 143
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1107
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 132
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1882
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 21085
bin: 7.5e0
variant carriers: 2

GenotypeDepth
all individuals: 138
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5903
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 709
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 177
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1529
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2951
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 176
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18496
bin: 1.25e1
variant carriers: 2

GenotypeDepth
all individuals: 1450
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 269
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 839
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 421
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2857
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 155
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1160
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32745
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6105
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2123
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 649
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2782
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5185
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 989
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 733
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 774
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4191
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1096
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 644
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 3
allele frequency: 6.139991813344249e-4
allele num: 4886
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 33852
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6438
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5996
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3550
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11372
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.04e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.11e-2

QD
type: SiteQuality
SIO_000300: 1.256e1

DP
type: SiteQuality
SIO_000300: 9.8383e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.7e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.66e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 1105
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 139
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10360
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1923
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 269
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 138
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 176
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1539
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1290
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1430
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 21641
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 16028
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1754
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 421
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 709
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 143
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 839
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 155
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 132
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10762
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1916
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4184
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 910
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2811
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 644
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 890
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27673
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2492
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 718
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2766
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2353
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10594
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.940993788819876e-4
allele num: 5152
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 460
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4006
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 27342
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5392
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3022
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.5e0

DP
type: SiteQuality
SIO_000300: 9.01473e5

MQRankSum
type: SiteQuality
SIO_000300: -5.29e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 8.84e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.97e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.646e0

GenotypeDepth
all individuals: 143
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 176
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 139
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 269
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1572
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1430
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1748
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 132
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 421
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 138
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 708
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1812
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 21652
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 15460
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 839
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1174
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1105
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 177
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 155
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 718
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2360
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2784
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26557
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2833
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4182
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 441
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 500
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11568
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2039
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 644
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2564
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 906
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 901
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3916
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2928
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5226
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.785297902944962e-5
allele num: 26418
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 446
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10466
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5028
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.758e0

VQSLOD
type: SiteQuality
SIO_000300: -4.834e-1

DP
type: SiteQuality
SIO_000300: 8.90733e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.09e-2

MQ
type: SiteQuality
SIO_000300: 5.947e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e0

QD
type: SiteQuality
SIO_000300: 1.487e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.482e0

MQRankSum
type: SiteQuality
SIO_000300: -1.388e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.709e0

GenotypeDepth
all individuals: 706
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9018
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 155
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 138
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1090
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 908
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 268
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 176
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1862
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 132
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13994
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1520
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1208
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 840
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 25502
bin: 7.5e0
variant carriers: 2

GenotypeDepth
all individuals: 142
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 139
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 177
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 422
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1176
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 736
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2491
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1913
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14384
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 637
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7759
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2319
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7144
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12879
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4179
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 639
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 232
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1053
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 702
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9368
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18354
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3878
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 356
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2590
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 3.054367745876604e-4
allele num: 3274
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2068
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.72e-1

FS
type: SiteQuality
SIO_000300: 1.889e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.99e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.10506e5

QD
type: SiteQuality
SIO_000300: 1.505e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.699e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

GenotypeDepth
all individuals: 268
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 177
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 991
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1482
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14060
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1083
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 840
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25841
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 1377
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1822
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1181
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 707
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 421
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 138
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 132
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 176
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 139
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 142
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 155
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14150
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 702
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2311
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4180
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 637
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2086
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7278
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 733
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 449
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8732
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11826
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 639
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1047
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1055
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2474
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3132
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3802
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 338
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 17842
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1986
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9284
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 7.62e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

DP
type: SiteQuality
SIO_000300: 8.0744e5

GenotypeDepth
all individuals: 176
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14118
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1190
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1795
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 8308
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 132
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26108
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1081
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1368
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 708
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1411
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 155
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 177
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 142
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 138
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 421
bin: 5.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 139
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 840
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10756
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2317
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2736
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 641
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2404
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13566
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 636
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4179
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 804
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9764
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7303
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1063
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 444
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 702
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 667
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9158
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2870
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 17218
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1878
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 336
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3684
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 4.266211604095563e-4
allele num: 2344
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.04988e5

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.717e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.14e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.141e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e0

QD
type: SiteQuality
SIO_000300: 5.44e0

GenotypeDepth
all individuals: 7391
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16793
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2874
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3793
bin: 2.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2162
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 624
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1834
bin: 5.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14255
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1585
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1325
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 832
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4289
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1151
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 938
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17848
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7532
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3266
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2816
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18232
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4974
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4060
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1909
bin: 8.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.939e1

MQRankSum
type: SiteQuality
SIO_000300: -2.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

VQSLOD
type: SiteQuality
SIO_000300: 8.1e-2

FS
type: SiteQuality
SIO_000300: 1.3e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.73e-1

QD
type: SiteQuality
SIO_000300: 1.681e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e0

DP
type: SiteQuality
SIO_000300: 2.36224e6

GenotypeDepth
all individuals: 24
bin: 1.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1151
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16805
bin: 2.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2162
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4286
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 624
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7391
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14252
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2872
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1325
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1584
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1834
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 832
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 347
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 938
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18227
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 17881
bin: 6.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7533
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3265
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4974
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4055
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1909
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2815
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 2.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 1.209e1

DP
type: SiteQuality
SIO_000300: 2.362156e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.849e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.09e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.812e0

QD
type: SiteQuality
SIO_000300: 1.085e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.0e-3

MQ
type: SiteQuality
SIO_000300: 5.983e1

GenotypeDepth
all individuals: 7391
bin: 3.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 831
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 347
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16812
bin: 2.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 14249
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1834
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2163
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1325
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 625
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 4284
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3809
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 938
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2872
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1583
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3265
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4051
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2815
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17905
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7532
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4972
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1908
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18227
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 2.12e0

DP
type: SiteQuality
SIO_000300: 2.362168e6

VQSLOD
type: SiteQuality
SIO_000300: -1.933e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

FS
type: SiteQuality
SIO_000300: 1.0646e1

MQ
type: SiteQuality
SIO_000300: 5.931e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.6e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.4e-1

QD
type: SiteQuality
SIO_000300: 1.062e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

GenotypeDepth
all individuals: 3809
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16812
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 474
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 14252
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1583
bin: 6.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2162
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 623
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1326
bin: 6.75e1
variant carriers: 1

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

GenotypeDepth
all individuals: 2871
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7391
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1835
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 347
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4285
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 832
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 937
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1151
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1908
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4051
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3263
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2814
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18227
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 4974
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17912
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7530
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 4
allele frequency: 4.622140050843541e-4
allele num: 8654
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: 11578
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.36225e6

MQ
type: SiteQuality
SIO_000300: 5.955e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.77e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.97e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.14e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.000000000000001e-2

FS
type: SiteQuality
SIO_000300: 5.37e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.3e-1

QD
type: SiteQuality
SIO_000300: 1.591e1

GenotypeDepth
all individuals: 1152
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1325
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 937
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1835
bin: 5.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 623
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7390
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1582
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4285
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 832
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2162
bin: 5.25e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 14250
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 347
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2871
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 474
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3813
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17919
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2814
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7532
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3263
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1908
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18223
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 2
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4973
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4051
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

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

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.585e0

DP
type: SiteQuality
SIO_000300: 2.36224e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.88e0

VQSLOD
type: SiteQuality
SIO_000300: -2.002e0

MQ
type: SiteQuality
SIO_000300: 5.923e1

MQRankSum
type: SiteQuality
SIO_000300: 2.85e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.65e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 9.92e-1

QD
type: SiteQuality
SIO_000300: 1.476e1

GenotypeDepth
all individuals: 1834
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16816
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 14250
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2871
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3814
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2162
bin: 5.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1581
bin: 6.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 624
bin: 8.25e1
variant carriers: 1

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

GenotypeDepth
all individuals: 1325
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1151
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 831
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 347
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 937
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7391
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4285
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4974
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3262
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18222
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4050
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17922
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1909
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2815
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7532
bin: 6.75e1
variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.63e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.42e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.29e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.342e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.29e0

QD
type: SiteQuality
SIO_000300: 1.647e1

DP
type: SiteQuality
SIO_000300: 2.362027e6

GenotypeDepth
all individuals: 831
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2163
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3814
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7391
bin: 3.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1834
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 347
bin: 9.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1582
bin: 6.25e1
variant carriers: 1

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

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

GenotypeDepth
all individuals: 1151
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1325
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2870
bin: 4.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 16817
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4284
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14250
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 937
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4050
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7532
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18222
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3263
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2814
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17921
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4974
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1909
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

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

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.278e0

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.137e1

MQRankSum
type: SiteQuality
SIO_000300: 8.74e-1

DP
type: SiteQuality
SIO_000300: 2.362001e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.06e-1

MQ
type: SiteQuality
SIO_000300: 5.942e1

FS
type: SiteQuality
SIO_000300: 4.85e-1

GenotypeDepth
all individuals: 16817
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14250
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 937
bin: 7.75e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 347
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2163
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 623
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3819
bin: 2.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2870
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1834
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1581
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7391
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4284
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 831
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1151
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1325
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4972
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1909
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7534
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18221
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17928
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2814
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4050
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3262
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

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

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 8.04e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.09e-1

FS
type: SiteQuality
SIO_000300: 5.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.942e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.86e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.67e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.117e0

DP
type: SiteQuality
SIO_000300: 2.362046e6

QD
type: SiteQuality
SIO_000300: 1.451e1

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

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

GenotypeDepth
all individuals: 2162
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 7.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 4284
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1835
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1150
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14250
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1581
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 623
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16814
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2870
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1325
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3821
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7392
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 831
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 937
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 347
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7533
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4051
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1909
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2814
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17928
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4972
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3262
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18220
bin: 9.75e1
variant carriers: 1

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -5.655e-1

QD
type: SiteQuality
SIO_000300: 9.94e0

MQRankSum
type: SiteQuality
SIO_000300: 8.24e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.608e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.34e-1

FS
type: SiteQuality
SIO_000300: 9.141e0

DP
type: SiteQuality
SIO_000300: 2.361966e6

MQ
type: SiteQuality
SIO_000300: 5.953e1

GenotypeDepth
all individuals: 16818
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14248
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1582
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1324
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3819
bin: 2.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 347
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 623
bin: 8.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1835
bin: 5.75e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 2869
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4284
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 937
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7392
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 830
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1151
bin: 7.25e1
variant carriers: 1

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

GenotypeDepth
all individuals: 2162
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3262
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4971
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1908
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4050
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17928
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2814
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18220
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7535
bin: 6.75e1
variant carriers: 0

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

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

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

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 8.94e-1

FS
type: SiteQuality
SIO_000300: 1.561e0

DP
type: SiteQuality
SIO_000300: 2.361874e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.59e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.235e1

MQRankSum
type: SiteQuality
SIO_000300: -3.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.85e-1

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

GenotypeDepth
all individuals: 2162
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 621
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1324
bin: 6.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 3819
bin: 2.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 14248
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1835
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 832
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 16818
bin: 2.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2868
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1582
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4283
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1150
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 347
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7392
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 937
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18217
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1908
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2814
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 7531
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17933
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3263
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4049
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4971
bin: 7.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.728011059270779e-4
allele num: 11574
num of homozygotes: 0

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

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.118e1

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.287e0

MQRankSum
type: SiteQuality
SIO_000300: -7.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 2.549e0

DP
type: SiteQuality
SIO_000300: 2.361794e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.97e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.06e-1

GenotypeDepth
all individuals: 1834
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14250
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1582
bin: 6.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1324
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 937
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16820
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 347
bin: 9.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 7387
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 830
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 621
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3812
bin: 2.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1150
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2160
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2868
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4281
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4966
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2812
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18212
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 4049
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1908
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7527
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17933
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3261
bin: 7.25e1
variant carriers: 0

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

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

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
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: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.616e0

MQRankSum
type: SiteQuality
SIO_000300: 1.49e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.51e0

DP
type: SiteQuality
SIO_000300: 2.361298e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.281e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.252e0

QD
type: SiteQuality
SIO_000300: 1.311e1

MQ
type: SiteQuality
SIO_000300: 5.969e1

FS
type: SiteQuality
SIO_000300: 9.987e0

GenotypeDepth
all individuals: 3815
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14242
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 937
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4276
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1834
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16801
bin: 2.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2160
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1582
bin: 6.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1325
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 34
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7384
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 830
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1149
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 621
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4045
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18208
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7520
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17926
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4959
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1906
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3255
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2810
bin: 9.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
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: 11572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.968e1

QD
type: SiteQuality
SIO_000300: 1.177e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 9.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.6e-1

DP
type: SiteQuality
SIO_000300: 2.360585e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.355e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

MQRankSum
type: SiteQuality
SIO_000300: 7.89e-1

GenotypeDepth
all individuals: 1582
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1150
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 829
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 347
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4276
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3812
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7383
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1325
bin: 6.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 16800
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2868
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2160
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 937
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1834
bin: 5.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 621
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1906
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3254
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17917
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18208
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 36
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2810
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7520
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4957
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4043
bin: 8.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
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: 1.498800959232614e-5
allele num: 66720
num of homozygotes: 0

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

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

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

QD
type: SiteQuality
SIO_000300: 1.099e1

DP
type: SiteQuality
SIO_000300: 2.360341e6

BaseQRankSum
type: SiteQuality
SIO_000300: -7.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.63e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.05e0

GenotypeDepth
all individuals: 2868
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4275
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14225
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7381
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 28
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1583
bin: 6.25e1
variant carriers: 3

GenotypeDepth
all individuals: 16790
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1152
bin: 7.25e1
variant carriers: 2

GenotypeDepth
all individuals: 1322
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3800
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 57
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1833
bin: 5.75e1
variant carriers: 3

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

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

GenotypeDepth
all individuals: 937
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 621
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 348
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2810
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18207
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 17893
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4042
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7518
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1905
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4955
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3250
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.593360995850622e-4
allele num: 11568
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.199184554502938e-4
allele num: 66712
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 8.599999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.63e-1

QD
type: SiteQuality
SIO_000300: 1.246e1

VQSLOD
type: SiteQuality
SIO_000300: 3.84e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.18e-1

FS
type: SiteQuality
SIO_000300: 6.56e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.527e0

DP
type: SiteQuality
SIO_000300: 2.35984e6

GenotypeDepth
all individuals: 16715
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4270
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14144
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3810
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1580
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2867
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 621
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 347
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2157
bin: 5.25e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 90
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7360
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1151
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 828
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1831
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1321
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 52
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4031
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18190
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 7474
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 49
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 63
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4931
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2802
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3237
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1902
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17773
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 1.92270717169775e-4
allele num: 10402
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66692
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.705e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.84e0

VQSLOD
type: SiteQuality
SIO_000300: -7.171e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.84e-1

FS
type: SiteQuality
SIO_000300: 1.197e0

DP
type: SiteQuality
SIO_000300: 2.355947e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.82e0

GenotypeDepth
all individuals: 2157
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1831
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 828
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16599
bin: 2.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2868
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 62
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 213
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 936
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1150
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 621
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1321
bin: 6.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 4247
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 346
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 347
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7287
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 80
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17610
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18189
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3188
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7302
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2799
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4017
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1901
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4886
bin: 7.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66652
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 5.513e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.830000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.55e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.05e-1

DP
type: SiteQuality
SIO_000300: 2.34963e6

QD
type: SiteQuality
SIO_000300: 9.23e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.96e-1

GenotypeDepth
all individuals: 4228
bin: 4.25e1
variant carriers: 3

GenotypeDepth
all individuals: 622
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2855
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 16576
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7218
bin: 3.75e1
variant carriers: 2

GenotypeDepth
all individuals: 73
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1829
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1151
bin: 7.25e1
variant carriers: 2

GenotypeDepth
all individuals: 1322
bin: 6.75e1
variant carriers: 2

GenotypeDepth
all individuals: 305
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1578
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 471
bin: 1.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 348
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2157
bin: 5.25e1
variant carriers: 4

GenotypeDepth
all individuals: 473
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 828
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 137
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4864
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1894
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17504
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 194
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18183
bin: 9.75e1
variant carriers: 23

GenotypeQuality
all individuals: 3996
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3154
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2788
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7246
bin: 6.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 22
allele frequency: 3.301518698601357e-4
allele num: 66636
num of homozygotes: 0

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

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

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

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

DP
type: SiteQuality
SIO_000300: 2.344105e6

VQSLOD
type: SiteQuality
SIO_000300: 3.34e0

MQRankSum
type: SiteQuality
SIO_000300: -2.62e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -5.1e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.22e0

QD
type: SiteQuality
SIO_000300: 1.412e1

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

GenotypeDepth
all individuals: 74
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3914
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1580
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 935
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 347
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4218
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2852
bin: 4.75e1
variant carriers: 2

GenotypeDepth
all individuals: 522
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 343
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7199
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1832
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1150
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13775
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 825
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 472
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 621
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1891
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17451
bin: 6.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 320
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7216
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 219
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18158
bin: 9.75e1
variant carriers: 5

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

GenotypeQuality
all individuals: 192
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2786
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3145
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4857
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3990
bin: 8.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.06134076857801e-5
allele num: 16498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66622
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 3.846893633391037e-4
allele num: 10398
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 2.58e0

QD
type: SiteQuality
SIO_000300: 1.389e1

FS
type: SiteQuality
SIO_000300: 1.836e0

MQRankSum
type: SiteQuality
SIO_000300: 2.03e-1

DP
type: SiteQuality
SIO_000300: 2.341514e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.49e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.958e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

GenotypeDepth
all individuals: 16354
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 347
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3987
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4168
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1150
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 826
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2149
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 935
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 676
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 836
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 107
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 13414
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 621
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1581
bin: 6.25e1
variant carriers: 2

GenotypeDepth
all individuals: 7081
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1320
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3125
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1889
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4833
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2787
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7040
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 462
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 223
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18150
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 16749
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3987
bin: 8.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.508409418548775e-5
allele num: 66592
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.56e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.277e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.328497e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.2e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.55e0

QD
type: SiteQuality
SIO_000300: 1.241e1