6-15651585-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15651585
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15651585
    reference: chr 6
allele count: 1
allele frequency: 8.244974687927709e-6
allele num: 121286
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+11460A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.120A>G
  hgvsp: ENST00000355917.3:c.120A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*118A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.*30A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.120A>G
  hgvsp: ENST00000338950.5:c.120A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.110+733A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.120A>G
  hgvsp: ENST00000344537.5:c.120A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*118A>G
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2244
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3880
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6725
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8675
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7937
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5316
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4869
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3472
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14871
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5060
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro40Pro
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

6-15651602-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15651602
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15651602
    reference: chr 6
allele count: 1
allele frequency: 8.245926512302922e-6
allele num: 121272
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*109-8T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*109-8T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.111-8T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.111-8T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.*13T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.111-8T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.110+716T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+11443T>C
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5316
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3880
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7934
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6726
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8675
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4868
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2239
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3471
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3348
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8534
  bin: 6.75e1
  variant carriers: 0
hgvs: c.111-8T>C
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ

6-15651603-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15651603
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15651603
    reference: chr 6
allele count: 1
allele frequency: 8.245790523937529e-6
allele num: 121274
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.*12T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.110+715T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*109-9T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.111-9T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+11442T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.111-9T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*109-9T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.111-9T>C
  variant of: http://identifiers.org/hgnc/17328
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3880
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4868
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2238
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6727
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7934
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5316
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8675
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3471
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14804
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8533
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3240
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19292
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

6-15651608-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15651608
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15651608
    reference: chr 6
allele count: 1
allele frequency: 8.247014580721778e-6
allele num: 121256
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.111-14T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+11437T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*109-14T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*109-14T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.111-14T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.111-14T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.110+710T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.*7T>C
  variant of: http://identifiers.org/hgnc/17328
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5315
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4869
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2223
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8673
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3880
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6727
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7926
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3470
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ

6-15651609-CACTTAT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15651609
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15651603
    reference: chr 6
allele count: 1
allele frequency: 8.246742536698004e-6
allele num: 121260
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*109-21_*109-16delATAAGT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.111-21_111-16delATAAGT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: coding_sequence_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.135_*5delATAAGT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.111-21_111-16delATAAGT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.110+703_110+708delATAAGT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.111-21_111-16delATAAGT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*109-21_*109-16delATAAGT
  variant of: http://identifiers.org/hgnc/17328
canonical: false
consequence: coding sequence
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4868
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8673
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6727
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2222
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3470
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7926
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5315
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3880
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3346
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14748
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
reference allele: CACTTAT
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ

6-15651615-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15651615
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15651615
    reference: chr 6
allele count: 1
allele frequency: 8.248239000973292e-6
allele num: 121238
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*109-21A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: stop_retained_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.135A>G
  hgvsp: ENST00000510395.1:c.135A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*109-21A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.111-21A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+11430A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.111-21A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.110+703A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.111-21A>G
  variant of: http://identifiers.org/hgnc/17328
canonical: false
consequence: stop retained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5315
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3470
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2206
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8673
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4865
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6725
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3880
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7924
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1930
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4269
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ter45Ter
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ

http://identifiers.org/exac.variant/6-15651618-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15651618
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15651618
    reference: chr 6
allele count: 1
allele frequency: 8.248102936324645e-6
allele num: 121240
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*109-24T>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*109-24T>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.132T>G
  hgvsp: ENSP00000424685.1:p.Phe44Leu
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.111-24T>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.110+700T>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.111-24T>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.111-24T>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+11427T>G
  variant of: http://identifiers.org/hgnc/17328
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6726
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4863
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3880
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2202
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3470
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5315
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7927
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8671
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5041
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1930
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Phe44Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

6-15651632-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15651632
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15651632
    reference: chr 6
allele count: 1
allele frequency: 8.263643275047103e-6
allele num: 121012
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.111-38A>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.110+686A>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*109-38A>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*109-38A>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.118A>C
  hgvsp: ENSP00000424685.1:p.Asn40His
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.111-38A>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+11413A>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.111-38A>C
  variant of: http://identifiers.org/hgnc/17328
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8517
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2849
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8237
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7568
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3470
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6702
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3877
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4335
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13136
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 571
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asn40His
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

6-15651636-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15651636
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15651636
    reference: chr 6
allele count: 1
allele frequency: 8.298617450332775e-6
allele num: 120502
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.114G>A
  hgvsp: ENSP00000424685.1:p.Trp38Ter
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.111-42G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+11409G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.111-42G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*109-42G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.111-42G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*109-42G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.110+682G>A
  variant of: http://identifiers.org/hgnc/17328
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6519
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3005
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3469
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3852
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4351
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2842
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7741
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6545
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6667
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1279
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Trp38Ter
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

6-15651639-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15651639
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15651639
    reference: chr 6
allele count: 2
allele frequency: 1.668724760537997e-5
allele num: 119852
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.111T>C
  hgvsp: ENST00000510395.1:c.111T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*109-45T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.111-45T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*109-45T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.110+679T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+11406T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.111-45T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.111-45T>C
  variant of: http://identifiers.org/hgnc/17328
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2385
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3851
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5269
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2818
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3786
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3470
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6078
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5072
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6959
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6545
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4454
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1340
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4141
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1253
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19225
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3162
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2961
  bin: 4.75e1
  variant carriers: 0
hgvs: c.111T>C
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

6-15651642-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15651642
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15651641
    reference: chr 6
allele count: 38826
allele frequency: 4.257143483695533e-1
allele num: 91202
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.111-49delT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.111-4delT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.111-49delT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+11402delT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*109-49delT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.111-49delT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*109-49delT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.110+675delT
  variant of: http://identifiers.org/hgnc/17328
canonical: false
consequence: splice region
filter: InbreedingCoeff_Filter
genotype depth: GenotypeDepth
  all individuals: 8950
  bin: 3.75e1
  variant carriers: 6600
genotype depth: GenotypeDepth
  all individuals: 5084
  bin: 2.25e1
  variant carriers: 3471
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 9.75e1
  variant carriers: 1589
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 7.5e0
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 1.25e1
  variant carriers: 419
genotype depth: GenotypeDepth
  all individuals: 2002
  bin: 5.75e1
  variant carriers: 1474
genotype depth: GenotypeDepth
  all individuals: 7879
  bin: 2.75e1
  variant carriers: 5617
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 8.25e1
  variant carriers: 727
genotype depth: GenotypeDepth
  all individuals: 2431
  bin: 1.75e1
  variant carriers: 1461
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 7.25e1
  variant carriers: 848
genotype depth: GenotypeDepth
  all individuals: 2948
  bin: 5.25e1
  variant carriers: 2253
genotype depth: GenotypeDepth
  all individuals: 4570
  bin: 4.75e1
  variant carriers: 3474
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9499
  bin: 3.25e1
  variant carriers: 6941
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 6.75e1
  variant carriers: 1055
genotype depth: GenotypeDepth
  all individuals: 6816
  bin: 4.25e1
  variant carriers: 5137
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 8.75e1
  variant carriers: 499
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 6.25e1
  variant carriers: 1190
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 9.25e1
  variant carriers: 388
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 7.75e1
  variant carriers: 775
genotype quality: GenotypeQuality
  all individuals: 2560
  bin: 1.75e1
  variant carriers: 1457
genotype quality: GenotypeQuality
  all individuals: 1991
  bin: 5.75e1
  variant carriers: 1699
genotype quality: GenotypeQuality
  all individuals: 2320
  bin: 4.25e1
  variant carriers: 1805
genotype quality: GenotypeQuality
  all individuals: 2446
  bin: 3.25e1
  variant carriers: 1730
genotype quality: GenotypeQuality
  all individuals: 2798
  bin: 2.25e1
  variant carriers: 1620
genotype quality: GenotypeQuality
  all individuals: 2374
  bin: 3.75e1
  variant carriers: 1780
genotype quality: GenotypeQuality
  all individuals: 1944
  bin: 5.25e1
  variant carriers: 1597
hgvs: c.111-4delT
num of homozygotes: 1
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: GA
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ

6-15651642-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15651642
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15651642
    reference: chr 6
allele count: 1
allele frequency: 1.096467182737221e-5
allele num: 91202
alternate allele: A
canonical: false
filter: InbreedingCoeff_Filter
genotype depth: GenotypeDepth
  all individuals: 2002
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4570
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5084
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2948
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8950
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7879
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2431
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9499
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6816
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2320
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2744
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2446
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1298
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2500
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2560
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2883
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1626
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6738
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2374
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15893
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1944
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1462
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1774
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2283
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1991
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1536
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2798
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1496
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2000
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 13190
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 5272
  num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 694
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7492
  num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD

6-15651642-G-GA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15651642
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15651643
    reference: chr 6
allele count: 3657
allele frequency: 4.009780487270016e-2
allele num: 91202
alternate allele: GA
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.110+675dupT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.111-49dupT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*109-49dupT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+11402dupT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.111-4dupT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.111-49dupT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.111-49dupT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*109-49dupT
  variant of: http://identifiers.org/hgnc/17328
canonical: false
consequence: splice region
filter: InbreedingCoeff_Filter
genotype depth: GenotypeDepth
  all individuals: 2431
  bin: 1.75e1
  variant carriers: 352
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 1.25e1
  variant carriers: 127
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 6.75e1
  variant carriers: 192
genotype depth: GenotypeDepth
  all individuals: 6816
  bin: 4.25e1
  variant carriers: 402
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 8.25e1
  variant carriers: 147
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 7.75e1
  variant carriers: 175
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 9.75e1
  variant carriers: 150
genotype depth: GenotypeDepth
  all individuals: 9499
  bin: 3.25e1
  variant carriers: 725
genotype depth: GenotypeDepth
  all individuals: 8950
  bin: 3.75e1
  variant carriers: 611
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 7.5e0
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5084
  bin: 2.25e1
  variant carriers: 634
genotype depth: GenotypeDepth
  all individuals: 4570
  bin: 4.75e1
  variant carriers: 255
genotype depth: GenotypeDepth
  all individuals: 7879
  bin: 2.75e1
  variant carriers: 739
genotype depth: GenotypeDepth
  all individuals: 2002
  bin: 5.75e1
  variant carriers: 178
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 9.25e1
  variant carriers: 76
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 8.75e1
  variant carriers: 101
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 6.25e1
  variant carriers: 204
genotype depth: GenotypeDepth
  all individuals: 2948
  bin: 5.25e1
  variant carriers: 188
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 7.25e1
  variant carriers: 203
genotype quality: GenotypeQuality
  all individuals: 6738
  bin: 2.5e0
  variant carriers: 409
genotype quality: GenotypeQuality
  all individuals: 2500
  bin: 2.75e1
  variant carriers: 402
genotype quality: GenotypeQuality
  all individuals: 1626
  bin: 7.25e1
  variant carriers: 110
genotype quality: GenotypeQuality
  all individuals: 1991
  bin: 5.75e1
  variant carriers: 176
genotype quality: GenotypeQuality
  all individuals: 2883
  bin: 7.5e0
  variant carriers: 493
genotype quality: GenotypeQuality
  all individuals: 2283
  bin: 4.75e1
  variant carriers: 262
genotype quality: GenotypeQuality
  all individuals: 1462
  bin: 8.75e1
  variant carriers: 82
hgvs: c.111-4dupT
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

6-15651642-G-GAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15651642
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15651644
    reference: chr 6
allele count: 14
allele frequency: 1.535054055832109e-4
allele num: 91202
alternate allele: GAA
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.110+674_110+675dupTT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.111-50_111-49dupTT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*109-50_*109-49dupTT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+11401_56+11402dupTT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.111-50_111-49dupTT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.111-5_111-4dupTT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.111-50_111-49dupTT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*109-50_*109-49dupTT
  variant of: http://identifiers.org/hgnc/17328
canonical: false
consequence: splice region
filter: InbreedingCoeff_Filter
genotype depth: GenotypeDepth
  all individuals: 9499
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2431
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6816
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5084
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7879
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8950
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2948
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4570
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2002
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1991
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2883
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6738
  bin: 2.5e0
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1774
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2374
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2283
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1462
  bin: 8.75e1
  variant carriers: 0
hgvs: c.111-5_111-4dupTT
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

6-15651642-GAA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15651642
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15651640
    reference: chr 6
allele count: 671
allele frequency: 7.357294796166751e-3
allele num: 91202
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.111-50_111-49delTT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*109-50_*109-49delTT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.111-5_111-4delTT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.111-50_111-49delTT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+11401_56+11402delTT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.111-50_111-49delTT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.110+674_110+675delTT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*109-50_*109-49delTT
  variant of: http://identifiers.org/hgnc/17328
canonical: false
consequence: splice region
filter: InbreedingCoeff_Filter
genotype depth: GenotypeDepth
  all individuals: 6816
  bin: 4.25e1
  variant carriers: 102
genotype depth: GenotypeDepth
  all individuals: 5084
  bin: 2.25e1
  variant carriers: 148
genotype depth: GenotypeDepth
  all individuals: 7879
  bin: 2.75e1
  variant carriers: 241
genotype depth: GenotypeDepth
  all individuals: 2948
  bin: 5.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 1.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 8.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 9499
  bin: 3.25e1
  variant carriers: 272
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4570
  bin: 4.75e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 2002
  bin: 5.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 6.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 6.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 8950
  bin: 3.75e1
  variant carriers: 193
genotype depth: GenotypeDepth
  all individuals: 2431
  bin: 1.75e1
  variant carriers: 60
genotype quality: GenotypeQuality
  all individuals: 1626
  bin: 7.25e1
  variant carriers: 28
genotype quality: GenotypeQuality
  all individuals: 2000
  bin: 6.25e1
  variant carriers: 42
genotype quality: GenotypeQuality
  all individuals: 1536
  bin: 7.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 2446
  bin: 3.25e1
  variant carriers: 97
genotype quality: GenotypeQuality
  all individuals: 2560
  bin: 1.75e1
  variant carriers: 72
genotype quality: GenotypeQuality
  all individuals: 1462
  bin: 8.75e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 2798
  bin: 2.25e1
  variant carriers: 61
hgvs: c.111-5_111-4delTT
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: GAA
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

6-15651642-GAAA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15651642
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15651639
    reference: chr 6
allele count: 8
allele frequency: 8.771737461897766e-5
allele num: 91202
alternate allele: G
canonical: false
filter: InbreedingCoeff_Filter
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2002
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7879
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2948
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9499
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5084
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2431
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4570
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6816
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8950
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2000
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2500
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2883
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1944
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2374
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2560
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2283
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 6738
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1462
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1496
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2744
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2798
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 15893
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1774
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2320
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1626
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1991
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1536
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1298
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2446
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 694
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 1
  allele frequency: 1.896813353566009e-4
  allele num: 5272
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 1
  allele frequency: 7.581501137225171e-5
  allele num: 13190
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6500
  num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
reference allele: GAAA
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

6-15651647-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15651647
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15651647
    reference: chr 6
allele count: 1
allele frequency: 8.397997917296517e-6
allele num: 119076
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.111-53T>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+11398T>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.110+671T>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.111-53T>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.111-8T>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*109-53T>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.111-53T>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*109-53T>A
  variant of: http://identifiers.org/hgnc/17328
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2613
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5021
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4667
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22509
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1786
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14803
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9258
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 4.75e1
  variant carriers: 0
hgvs: c.111-8T>A
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ

6-15651650-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15651650
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15651650
    reference: chr 6
allele count: 1
allele frequency: 8.422471153036301e-6
allele num: 118730
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*109-56T>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.111-56T>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.111-56T>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.110+668T>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+11395T>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*109-56T>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.111-11T>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.111-56T>A
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2605
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1784
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22119
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4849
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14666
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4657
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2763
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2667
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 829
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1701
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum

6-15651673-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15651673
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15651673
    reference: chr 6
allele count: 1
allele frequency: 8.67995278105687e-6
allele num: 115208
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.111-79A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.111-79A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*109-79A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+11372A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*109-79A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.111-79A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.111-34A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.110+645A>G
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8968
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6653
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15613
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4138
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1945
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3411
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9828
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6472
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2696
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7683
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1738
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

6-15651677-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15651677
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15651677
    reference: chr 6
allele count: 1
allele frequency: 8.824567596187787e-6
allele num: 113320
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.111-83T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*109-83T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.110+641T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.111-38T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.111-83T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*109-83T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.111-83T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+11368T>C
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12608
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7858
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11035
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4477
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2503
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8836
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1870
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3167
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 610
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1778
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5487
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 511
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 500
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1715
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

6-15651678-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15651678
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15651678
    reference: chr 6
allele count: 1
allele frequency: 8.813678829543451e-6
allele num: 113460
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.110+640A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+11367A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.111-84A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.111-39A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*109-84A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.111-84A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*109-84A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.111-84A>G
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4513
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7800
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11054
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12608
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2523
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3147
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8847
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1866
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1474
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4571
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3239
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 482
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1867
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1701
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD

6-15651682-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15651682
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15651682
    reference: chr 6
allele count: 1
allele frequency: 8.914721771533511e-6
allele num: 112174
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.111-43G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.110+636G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.111-88G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.111-88G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*109-88G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.111-88G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+11363G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*109-88G>A
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9302
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2987
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2979
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8645
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12455
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7509
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6606
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2900
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1503
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 708
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 877
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7105
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3308
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 697
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum

6-15651687-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15651687
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15651687
    reference: chr 6
allele count: 4
allele frequency: 3.637091054574551e-5
allele num: 109978
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.110+631C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*109-93C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.111-93C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.111-48C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.111-93C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+11358C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.111-93C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*109-93C>T
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8456
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4982
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12121
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1820
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2745
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10683
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7901
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3577
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 996
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1554
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6152
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2507
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7386
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1452
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5963
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD

6-15651688-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15651688
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15651688
    reference: chr 6
allele count: 105
allele frequency: 9.716644148729433e-4
allele num: 108062
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*109-94A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+11357A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.111-94A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*109-94A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.111-94A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.111-94A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.110+630A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.111-49A>G
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8435
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 12011
  bin: 1.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4468
  bin: 3.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 11334
  bin: 2.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3728
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2655
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7823
  bin: 2.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 551
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4614
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5458
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5052
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1689
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1157
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1466
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

6-15652267-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15652267
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15652267
    reference: chr 6
allele count: 1
allele frequency: 8.266375690242371e-6
allele num: 120972
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.110+51C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*108+51C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.110+51C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.110+51C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*108+51C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.110+51C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+10778C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.110+51C>T
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19327
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6745
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17161
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7704
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1910
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3221
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2468
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1824
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

6-15652270-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15652270
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15652270
    reference: chr 6
allele count: 1
allele frequency: 8.267742575567167e-6
allele num: 120952
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.110+48C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.110+48C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.110+48C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.110+48C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.110+48C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*108+48C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*108+48C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+10775C>T
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17139
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19362
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7702
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6903
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3219
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 841
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9822
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-15652273-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15652273
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15652273
    reference: chr 6
allele count: 23
allele frequency: 1.901234976110569e-4
allele num: 120974
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.110+45A>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.110+45A>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.110+45A>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+10772A>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*108+45A>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*108+45A>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.110+45A>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.110+45A>C
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19436
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17123
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7122
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3222
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7689
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2555
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 712
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2457
  bin: 9.75e1
  variant carriers: 23
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: T
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

6-15652284-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15652284
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15652284
    reference: chr 6
allele count: 2
allele frequency: 1.65305650147122e-5
allele num: 120988
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.110+34A>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.110+34A>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.110+34A>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.110+34A>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+10761A>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*108+34A>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*108+34A>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.110+34A>T
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19594
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17106
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7686
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7744
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 580
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9773
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1705
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: QD

http://identifiers.org/exac.variant/6-15652285-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15652285
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15652285
    reference: chr 6
allele count: 2
allele frequency: 1.65338447802652e-5
allele num: 120964
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+10760G>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*108+33G>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*108+33G>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.110+33G>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.110+33G>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.110+33G>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.110+33G>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.110+33G>T
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7689
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7770
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19616
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17120
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 578
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2515
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2433
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

6-15652285-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15652285
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15652285
    reference: chr 6
allele count: 2
allele frequency: 1.65338447802652e-5
allele num: 120964
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*108+33G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+10760G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.110+33G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.110+33G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*108+33G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.110+33G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.110+33G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.110+33G>A
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19616
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17120
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7689
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7770
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2433
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD

6-15652287-CAGTTA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15652287
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15652282
    reference: chr 6
allele count: 2
allele frequency: 1.653220473482343e-5
allele num: 120976
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.110+26_110+30delTAACT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.110+26_110+30delTAACT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.110+26_110+30delTAACT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*108+26_*108+30delTAACT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.110+26_110+30delTAACT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.110+26_110+30delTAACT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*108+26_*108+30delTAACT
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17118
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7689
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7859
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19662
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9757
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 779
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2507
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2431
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: CAGTTA
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD

6-15652289-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15652289
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15652289
    reference: chr 6
allele count: 2
allele frequency: 1.653247805313538e-5
allele num: 120974
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.110+29C>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*108+29C>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.110+29C>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.110+29C>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.110+29C>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.110+29C>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*108+29C>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+10756C>A
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7941
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17130
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19685
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7689
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2429
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 576
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2502
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: DP
site quality: QD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff

6-15652301-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15652301
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15652301
    reference: chr 6
allele count: 3
allele frequency: 2.479092982514131e-5
allele num: 121012
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.110+17A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.110+17A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*108+17A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*108+17A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.110+17A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+10744A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.110+17A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.110+17A>G
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19832
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7690
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17112
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3207
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8398
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1688
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2426
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 39191
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ

6-15652312-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15652312
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15652312
    reference: chr 6
allele count: 1
allele frequency: 8.262277744728666e-6
allele num: 121032
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*108+6C>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.110+6C>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.110+6C>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.110+6C>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.110+6C>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+10733C>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.110+6C>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*108+6C>A
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7683
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8536
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17135
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3206
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19934
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2422
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9780
  bin: 6.75e1
  variant carriers: 0
hgvs: c.110+6C>A
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

6-15652320-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15652320
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15652320
    reference: chr 6
allele count: 2
allele frequency: 1.652810604432838e-5
allele num: 121006
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.108C>G
  hgvsp: ENST00000344537.5:c.108C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*106C>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.108C>G
  hgvsp: ENST00000338950.5:c.108C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.108C>G
  hgvsp: ENST00000515875.1:c.108C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.108C>G
  hgvsp: ENST00000355917.3:c.108C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.108C>G
  hgvsp: ENST00000510395.1:c.108C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+10725C>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*106C>G
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7686
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19990
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8429
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17142
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1691
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9771
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
hgvs: c.108C>G
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

6-15652320-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15652320
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15652320
    reference: chr 6
allele count: 2
allele frequency: 1.652810604432838e-5
allele num: 121006
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.108C>A
  hgvsp: ENST00000515875.1:c.108C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.108C>A
  hgvsp: ENST00000344537.5:c.108C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*106C>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+10725C>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*106C>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.108C>A
  hgvsp: ENST00000338950.5:c.108C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.108C>A
  hgvsp: ENST00000355917.3:c.108C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.108C>A
  hgvsp: ENST00000510395.1:c.108C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19990
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8429
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7686
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17142
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9771
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: c.108C>A
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP

6-15652333-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15652333
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15652333
    reference: chr 6
allele count: 1
allele frequency: 8.275131574592036e-6
allele num: 120844
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+10712T>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*93T>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.95T>A
  hgvsp: ENSP00000341680.5:p.Val32Glu
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.95T>A
  hgvsp: ENSP00000424685.1:p.Val32Glu
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*93T>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.95T>A
  hgvsp: ENSP00000348183.3:p.Val32Glu
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.95T>A
  hgvsp: ENSP00000425495.1:p.Val32Glu
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.95T>A
  hgvsp: ENSP00000344718.5:p.Val32Glu
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17126
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7676
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8100
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20020
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2418
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 620
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val32Glu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

6-15652340-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15652340
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15652340
    reference: chr 6
allele count: 9
allele frequency: 7.465038735256548e-5
allele num: 120562
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.88G>A
  hgvsp: ENSP00000424685.1:p.Ala30Thr
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+10705G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*86G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.88G>A
  hgvsp: ENSP00000341680.5:p.Ala30Thr
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*86G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.88G>A
  hgvsp: ENSP00000344718.5:p.Ala30Thr
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.88G>A
  hgvsp: ENSP00000425495.1:p.Ala30Thr
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.88G>A
  hgvsp: ENSP00000348183.3:p.Ala30Thr
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3207
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7678
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7514
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19853
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17078
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38415
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9631
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala30Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

6-15652344-TCTTGA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15652344
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15652339
    reference: chr 6
allele count: 23
allele frequency: 1.909410905226805e-4
allele num: 120456
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*77_*81delTCAAG
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.79_83delTCAAG
  hgvsp: ENSP00000348183.3:p.Ser27ArgfsTer25
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.79_83delTCAAG
  hgvsp: ENSP00000344718.5:p.Ser27ArgfsTer25
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.79_83delTCAAG
  hgvsp: ENSP00000424685.1:p.Ser27ArgfsTer40
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*77_*81delTCAAG
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.79_83delTCAAG
  hgvsp: ENSP00000341680.5:p.Ser27ArgfsTer25
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.79_83delTCAAG
  hgvsp: ENSP00000425495.1:p.Ser27ArgfsTer11
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17029
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19768
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7667
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7292
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3206
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2902
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser27ArgfsTer25
num of homozygotes: 1
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: TCTTGA
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

6-15652351-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15652351
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15652351
    reference: chr 6
allele count: 1
allele frequency: 8.324315325064513e-6
allele num: 120130
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*75A>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.77A>T
  hgvsp: ENSP00000424685.1:p.Lys26Met
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.77A>T
  hgvsp: ENSP00000344718.5:p.Lys26Met
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+10694A>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.77A>T
  hgvsp: ENSP00000348183.3:p.Lys26Met
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*75A>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.77A>T
  hgvsp: ENSP00000341680.5:p.Lys26Met
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.77A>T
  hgvsp: ENSP00000425495.1:p.Lys26Met
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19495
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6689
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3201
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7654
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16938
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9447
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2330
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37468
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Lys26Met
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

6-15652358-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15652358
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15652358
    reference: chr 6
allele count: 2
allele frequency: 1.675771692864564e-5
allele num: 119348
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.70A>C
  hgvsp: ENSP00000424685.1:p.Ser24Arg
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.70A>C
  hgvsp: ENSP00000425495.1:p.Ser24Arg
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*68A>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.70A>C
  hgvsp: ENSP00000348183.3:p.Ser24Arg
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.70A>C
  hgvsp: ENSP00000344718.5:p.Ser24Arg
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*68A>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.70A>C
  hgvsp: ENSP00000341680.5:p.Ser24Arg
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+10687A>C
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16633
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7597
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18587
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2769
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3194
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5593
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 551
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4145
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser24Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: African
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum

6-15652358-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15652358
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15652358
    reference: chr 6
allele count: 1
allele frequency: 8.37885846432282e-6
allele num: 119348
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.70A>T
  hgvsp: ENSP00000425495.1:p.Ser24Cys
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.70A>T
  hgvsp: ENSP00000348183.3:p.Ser24Cys
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.70A>T
  hgvsp: ENSP00000341680.5:p.Ser24Cys
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.70A>T
  hgvsp: ENSP00000424685.1:p.Ser24Cys
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*68A>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+10687A>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*68A>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.70A>T
  hgvsp: ENSP00000344718.5:p.Ser24Cys
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3194
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7597
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2769
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18587
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5593
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16633
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1582
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4145
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser24Cys
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

6-15652360-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15652360
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15652360
    reference: chr 6
allele count: 1
allele frequency: 8.417508417508417e-6
allele num: 118800
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.68T>C
  hgvsp: ENSP00000348183.3:p.Leu23Ser
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.68T>C
  hgvsp: ENSP00000341680.5:p.Leu23Ser
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.68T>C
  hgvsp: ENSP00000344718.5:p.Leu23Ser
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+10685T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*66T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*66T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.68T>C
  hgvsp: ENSP00000425495.1:p.Leu23Ser
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.68T>C
  hgvsp: ENSP00000424685.1:p.Leu23Ser
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16445
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5024
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3190
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17881
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3317
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2202
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7567
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2712
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8863
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1575
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 759
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu23Ser
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: Latino
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD

6-15652363-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15652363
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15652363
    reference: chr 6
allele count: 1
allele frequency: 8.487235198261813e-6
allele num: 117824
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.65C>T
  hgvsp: ENSP00000348183.3:p.Thr22Ile
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.65C>T
  hgvsp: ENSP00000344718.5:p.Thr22Ile
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+10682C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*63C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.65C>T
  hgvsp: ENSP00000341680.5:p.Thr22Ile
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.65C>T
  hgvsp: ENSP00000425495.1:p.Thr22Ile
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.65C>T
  hgvsp: ENSP00000424685.1:p.Thr22Ile
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*63C>T
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4571
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3177
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16112
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7516
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16801
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 757
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1563
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6765
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr22Ile
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

6-15652380-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15652380
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15652380
    reference: chr 6
allele count: 1
allele frequency: 1.155187949079315e-5
allele num: 86566
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*55-9G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.57-9G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.57-9G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.57-9G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*55-9G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.57-9G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+10665G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.57-9G>A
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4529
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3113
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11380
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4952
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17903
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6740
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5343
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2660
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1033
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28613
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2919
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-15652385-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15652385
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15652385
    reference: chr 6
allele count: 3
allele frequency: 4.234895539243365e-5
allele num: 70840
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.57-14A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.57-14A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.57-14A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*55-14A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.57-14A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*55-14A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.57-14A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+10660A>G
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2012
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5081
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13693
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1723
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18736
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9279
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 839
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 385
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7604
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

6-15652394-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15652394
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15652394
    reference: chr 6
allele count: 7
allele frequency: 1.187769369124784e-4
allele num: 58934
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.57-23T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.57-23T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*55-23T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+10651T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*55-23T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.57-23T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.57-23T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.57-23T>C
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3473
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16446
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14060
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13551
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2644
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1833
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 898
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1330
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 733
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 923
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1463
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

6-15652395-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15652395
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15652395
    reference: chr 6
allele count: 1
allele frequency: 1.69600759811404e-5
allele num: 58962
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.57-24A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.57-24A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*55-24A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*55-24A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.57-24A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.57-24A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.57-24A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+10650A>G
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13608
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14078
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1586
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3475
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16430
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14812
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 900
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 733
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 722
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24612
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum

6-15652400-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15652400
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15652400
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 52066
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*55-29A>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*55-29A>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.57-29A>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+10645A>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.57-29A>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.57-29A>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.57-29A>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.57-29A>T
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14121
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15827
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14312
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1853
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20784
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 530
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1404
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 508
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1764
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-15652406-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15652406
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15652406
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 44622
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.57-35C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*55-35C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.57-35C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.57-35C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*55-35C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.57-35C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.57-35C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+10639C>T
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 17034
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11078
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15551
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2279
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3424
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1794
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16480
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 729
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1659
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

6-15652413-GATT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15652413
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15652410
    reference: chr 6
allele count: 1
allele frequency: 2.519018590357197e-5
allele num: 39698
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+10629_56+10631delAAT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.57-45_57-43delAAT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.57-45_57-43delAAT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*55-45_*55-43delAAT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.57-45_57-43delAAT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*55-45_*55-43delAAT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.57-45_57-43delAAT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.57-45_57-43delAAT
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8753
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17069
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2020
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3338
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 719
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12809
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4088
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17705
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: GATT
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

6-15660583-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15660583
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15660583
    reference: chr 6
allele count: 130
allele frequency: 1.055023535140399e-2
allele num: 12322
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*54+31G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.56+2462G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.56+2462G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*54+31G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+2462G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.56+2462G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.56+2462G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.56+2462G>A
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 3.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.5e0
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1911
  bin: 2.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.75e1
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 4.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1500
  bin: 7.5e0
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 5
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD

6-15660585-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15660585
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15660585
    reference: chr 6
allele count: 4
allele frequency: 3.246753246753247e-4
allele num: 12320
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.56+2460C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.56+2460C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.56+2460C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.56+2460C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*54+29C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.56+2460C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+2460C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*54+29C>T
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2814
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1550
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

6-15660625-GAAC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15660625
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15660622
    reference: chr 6
allele count: 3
allele frequency: 2.435460301997078e-4
allele num: 12318
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.56+2417_56+2419delGTT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.56+2417_56+2419delGTT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.56+2417_56+2419delGTT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*40_*42delGTT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.56+2417_56+2419delGTT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*40_*42delGTT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.56+2417_56+2419delGTT
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+2417_56+2419delGTT
  variant of: http://identifiers.org/hgnc/17328
canonical: false
consequence: 3' UTR
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: GAAC
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

6-15660646-CG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15660646
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15660645
    reference: chr 6
allele count: 1
allele frequency: 8.124796880077999e-5
allele num: 12308
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.56+2398delC
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.56+2398delC
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.56+2398delC
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.56+2398delC
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*21delC
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.56+2398delC
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+2398delC
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*21delC
  variant of: http://identifiers.org/hgnc/17328
canonical: false
consequence: 3' UTR
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2808
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1026
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: African
population: East Asian
reference allele: CG
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

6-15660658-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15660658
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15660658
    reference: chr 6
allele count: 1
allele frequency: 8.127438231469441e-5
allele num: 12304
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.56+2387C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.56+2387C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+2387C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.*10C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.56+2387C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.56+2387C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.*10C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.56+2387C>T
  variant of: http://identifiers.org/hgnc/17328
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1972
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1028
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

6-15660715-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15660715
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15660715
    reference: chr 6
allele count: 1
allele frequency: 8.206138191367142e-5
allele num: 12186
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.56+2330G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.56+2330G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.56+2330G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.94G>A
  hgvsp: ENSP00000424357.1:p.Val32Met
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.56+2330G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+2330G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.56+2330G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.94G>A
  hgvsp: ENSP00000424202.1:p.Val32Met
  variant of: http://identifiers.org/hgnc/17328
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1843
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2805
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Val32Met
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ

6-15660718-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15660718
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15660718
    reference: chr 6
allele count: 1
allele frequency: 8.227743952608195e-5
allele num: 12154
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.56+2327T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.56+2327T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.91T>C
  hgvsp: ENSP00000424202.1:p.Cys31Arg
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.56+2327T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+2327T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.56+2327T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.91T>C
  hgvsp: ENSP00000424357.1:p.Cys31Arg
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.56+2327T>C
  variant of: http://identifiers.org/hgnc/17328
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2045
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1833
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 447
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 948
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Cys31Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

6-15660771-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15660771
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15660771
    reference: chr 6
allele count: 47
allele frequency: 4.006820119352088e-3
allele num: 11730
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.57-19T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.56+2274T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.56+2274T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.56+2274T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.56+2274T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+2274T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.57-19T>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.56+2274T>C
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2124
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1818
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 447
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 549
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 3.25e1
  variant carriers: 1
num of homozygotes: 3
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD

6-15662997-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15662997
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15662997
    reference: chr 6
allele count: 2
allele frequency: 1.712270127735352e-5
allele num: 116804
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.56+48C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.56+48C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.56+48C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+48C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.56+48C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.56+48C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.56+48C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.56+48C>T
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3338
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2069
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6338
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10743
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18790
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 509
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 680
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28155
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 574
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ

6-15663002-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15663002
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15663002
    reference: chr 6
allele count: 1
allele frequency: 8.564870327863236e-6
allele num: 116756
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.56+43G>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.56+43G>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.56+43G>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+43G>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.56+43G>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.56+43G>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.56+43G>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.56+43G>C
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18919
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6488
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2069
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3346
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10788
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 594
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 474
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7411
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1606
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

6-15663006-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15663006
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15663006
    reference: chr 6
allele count: 4
allele frequency: 3.424950766332734e-5
allele num: 116790
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.56+39G>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.56+39G>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.56+39G>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.56+39G>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.56+39G>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.56+39G>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+39G>C
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.56+39G>C
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3356
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10829
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6642
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19069
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1852
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2071
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1448
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15400
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: African
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ

6-15663010-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15663010
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15663010
    reference: chr 6
allele count: 2
allele frequency: 1.710629853912211e-5
allele num: 116916
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.56+35G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.56+35G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.56+35G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.56+35G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.56+35G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.56+35G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+35G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.56+35G>A
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3356
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10845
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6887
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2069
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19151
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 601
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1462
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7522
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD

6-15663016-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15663016
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15663016
    reference: chr 6
allele count: 1
allele frequency: 8.554173581290312e-6
allele num: 116902
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.56+29A>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.56+29A>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.56+29A>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.56+29A>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.56+29A>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.56+29A>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+29A>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.56+29A>T
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19247
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10871
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7039
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3370
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1459
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum

6-15663016-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15663016
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15663016
    reference: chr 6
allele count: 4
allele frequency: 3.421669432516125e-5
allele num: 116902
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.56+29A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.56+29A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.56+29A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.56+29A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.56+29A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+29A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.56+29A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.56+29A>G
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19247
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7039
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3370
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10871
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1824
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 544
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

6-15663020-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15663020
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15663020
    reference: chr 6
allele count: 1
allele frequency: 8.543649505322693e-6
allele num: 117046
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.56+25A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+25A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.56+25A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.56+25A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.56+25A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.56+25A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.56+25A>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.56+25A>G
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2069
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7167
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10882
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19311
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3375
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1855
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7557
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1469
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29825
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQ

6-15663024-CG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15663024
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15663023
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 117032
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.56+20delC
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.56+20delC
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.56+20delC
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.56+20delC
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.56+20delC
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.56+20delC
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.56+20delC
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+20delC
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2069
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7159
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19330
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1426
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3373
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10892
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1474
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7564
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 672
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: East Asian
reference allele: CG
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP

6-15663028-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15663028
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15663028
    reference: chr 6
allele count: 2
allele frequency: 1.708642312818235e-5
allele num: 117052
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.56+17C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.56+17C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.56+17C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+17C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.56+17C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.56+17C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.56+17C>T
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.56+17C>T
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10900
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7158
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3381
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19356
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2070
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1631
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29795
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP

6-15663028-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15663028
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15663028
    reference: chr 6
allele count: 2
allele frequency: 1.708642312818235e-5
allele num: 117052
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+17C>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.56+17C>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.56+17C>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.56+17C>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.56+17C>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.56+17C>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.56+17C>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.56+17C>A
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10900
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3381
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7158
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19356
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2070
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7577
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1466
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1963
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ

http://identifiers.org/exac.variant/6-15663032-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15663032
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15663032
    reference: chr 6
allele count: 1
allele frequency: 8.536502082906508e-6
allele num: 117144
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.56+13T>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+13T>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.56+13T>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.56+13T>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.56+13T>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.56+13T>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.56+13T>G
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.56+13T>G
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10906
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2069
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7253
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3378
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19388
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1629
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD

6-15663034-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15663034
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 15663034
    reference: chr 6
allele count: 1
allele frequency: 8.535919147773831e-6
allele num: 117152
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000348183
  ensembl transcript: ENST00000355917
  gene symbol: DTNBP1
  hgvsc: ENST00000355917.3:c.56+11G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424685
  ensembl transcript: ENST00000510395
  gene symbol: DTNBP1
  hgvsc: ENST00000510395.1:c.56+11G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424202
  ensembl transcript: ENST00000506844
  gene symbol: DTNBP1
  hgvsc: ENST00000506844.1:c.56+11G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000427473
  ensembl transcript: ENST00000511762
  gene symbol: DTNBP1
  hgvsc: ENST00000511762.2:c.56+11G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000341680
  ensembl transcript: ENST00000344537
  gene symbol: DTNBP1
  hgvsc: ENST00000344537.5:c.56+11G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000424357
  ensembl transcript: ENST00000513680
  gene symbol: DTNBP1
  hgvsc: ENST00000513680.1:c.56+11G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000425495
  ensembl transcript: ENST00000515875
  gene symbol: DTNBP1
  hgvsc: ENST00000515875.1:c.56+11G>A
  variant of: http://identifiers.org/hgnc/17328
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000047579
  ensembl protein: ENSP00000344718
  ensembl transcript: ENST00000338950
  gene symbol: DTNBP1
  hgvsc: ENST00000338950.5:c.56+11G>A
  variant of: http://identifiers.org/hgnc/17328
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7231
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10911
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19398
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2069
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3376
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29953
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1469
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 86
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3246
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4274
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8543
bin: 6.75e1
variant carriers: 0

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

Other
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European (Non-Finnish)
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South Asian
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Latino
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East Asian
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African
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DP
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MQRankSum
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QD
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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FS
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ClippingRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Non-Finnish)
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South Asian
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Other
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Latino
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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DP
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VQSLOD
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ReadPosRankSum
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QD
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FS
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InbreedingCoeff
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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Latino
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African
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East Asian
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South Asian
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European (Finnish)
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MQ
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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FS
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QD
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VQSLOD
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DP
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ClippingRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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South Asian
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Latino
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InbreedingCoeff
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FS
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DP
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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MQ
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QD
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VQSLOD
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European (Non-Finnish)
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African
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East Asian
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European (Finnish)
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DP
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ReadPosRankSum
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MQ
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FS
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MQRankSum
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InbreedingCoeff
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VQSLOD
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QD
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GenotypeQuality
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GenotypeQuality
all individuals: 6466
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3327
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 814
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2436
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4841
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 578
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.032232632887595e-5
allele num: 65958
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10032
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11462
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8400
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.51e-1

FS
type: SiteQuality
SIO_000300: 3.661e0

DP
type: SiteQuality
SIO_000300: 3.384455e6

VQSLOD
type: SiteQuality
SIO_000300: 6.53e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.699999999999999e-3

MQ
type: SiteQuality
SIO_000300: 5.931e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

QD
type: SiteQuality
SIO_000300: 1.249e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.201e0

GenotypeQuality
all individuals: 1774
bin: 6.75e1
variant carriers: 1534

GenotypeQuality
all individuals: 2883
bin: 7.5e0
variant carriers: 1189

GenotypeQuality
all individuals: 2744
bin: 1.25e1
variant carriers: 1430

GenotypeQuality
all individuals: 2000
bin: 6.25e1
variant carriers: 1621

GenotypeQuality
all individuals: 2283
bin: 4.75e1
variant carriers: 1834

GenotypeQuality
all individuals: 6738
bin: 2.5e0
variant carriers: 1023

GenotypeQuality
all individuals: 15893
bin: 9.75e1
variant carriers: 15266

GenotypeQuality
all individuals: 1536
bin: 7.75e1
variant carriers: 1392

GenotypeQuality
all individuals: 2500
bin: 2.75e1
variant carriers: 1616

GenotypeQuality
all individuals: 1626
bin: 7.25e1
variant carriers: 1460

GenotypeQuality
all individuals: 1298
bin: 9.25e1
variant carriers: 1221

GenotypeQuality
all individuals: 1496
bin: 8.25e1
variant carriers: 1361

GenotypeQuality
all individuals: 1462
bin: 8.75e1
variant carriers: 1353

East Asian
type: Population
allele count: 2884
allele frequency: 4.436923076923077e-1
allele num: 6500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 21258
allele frequency: 4.294198448610213e-1
allele num: 49504
num of homozygotes: 0

African
type: Population
allele count: 3224
allele frequency: 4.303256807261078e-1
allele num: 7492
num of homozygotes: 0

Latino
type: Population
allele count: 3678
allele frequency: 4.301754385964912e-1
allele num: 8550
num of homozygotes: 1

Other
type: Population
allele count: 296
allele frequency: 4.265129682997118e-1
allele num: 694
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2291
allele frequency: 4.345599393019727e-1
allele num: 5272
num of homozygotes: 0

South Asian
type: Population
allele count: 5195
allele frequency: 3.938589840788476e-1
allele num: 13190
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.591e-1

QD
type: SiteQuality
SIO_000300: 1.8e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.45e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.55e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.46e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.59e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.56379e6

MQ
type: SiteQuality
SIO_000300: 5.969e1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6500
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.169590643274854e-4
allele num: 8550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 49504
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.591e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.45e-1

DP
type: SiteQuality
SIO_000300: 2.56379e6

QD
type: SiteQuality
SIO_000300: 1.8e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.55e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.59e0

GenotypeQuality
all individuals: 2446
bin: 3.25e1
variant carriers: 296

GenotypeQuality
all individuals: 2374
bin: 3.75e1
variant carriers: 289

GenotypeQuality
all individuals: 2320
bin: 4.25e1
variant carriers: 293

GenotypeQuality
all individuals: 2000
bin: 6.25e1
variant carriers: 175

GenotypeQuality
all individuals: 15893
bin: 9.75e1
variant carriers: 551

GenotypeQuality
all individuals: 1496
bin: 8.25e1
variant carriers: 103

GenotypeQuality
all individuals: 2798
bin: 2.25e1
variant carriers: 426

GenotypeQuality
all individuals: 2744
bin: 1.25e1
variant carriers: 446

GenotypeQuality
all individuals: 1298
bin: 9.25e1
variant carriers: 60

GenotypeQuality
all individuals: 1536
bin: 7.75e1
variant carriers: 101

GenotypeQuality
all individuals: 2560
bin: 1.75e1
variant carriers: 455

GenotypeQuality
all individuals: 1774
bin: 6.75e1
variant carriers: 137

GenotypeQuality
all individuals: 1944
bin: 5.25e1
variant carriers: 212

European (Non-Finnish)
type: Population
allele count: 1662
allele frequency: 3.357304460245637e-2
allele num: 49504
num of homozygotes: 0

Other
type: Population
allele count: 28
allele frequency: 4.034582132564841e-2
allele num: 694
num of homozygotes: 0

East Asian
type: Population
allele count: 173
allele frequency: 2.661538461538461e-2
allele num: 6500
num of homozygotes: 0

Latino
type: Population
allele count: 343
allele frequency: 4.011695906432749e-2
allele num: 8550
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 54
allele frequency: 1.024279210925645e-2
allele num: 5272
num of homozygotes: 0

African
type: Population
allele count: 247
allele frequency: 3.296849973304859e-2
allele num: 7492
num of homozygotes: 0

South Asian
type: Population
allele count: 1150
allele frequency: 8.718726307808947e-2
allele num: 13190
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.56379e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.45e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.46e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.05e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.59e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.591e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

QD
type: SiteQuality
SIO_000300: 1.8e0

GenotypeQuality
all individuals: 2320
bin: 4.25e1
variant carriers: 4

GenotypeQuality
all individuals: 2560
bin: 1.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2744
bin: 1.25e1
variant carriers: 3

GenotypeQuality
all individuals: 1944
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2798
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2000
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1298
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1626
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2500
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 15893
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1496
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1536
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2446
bin: 3.25e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.414027149321267e-4
allele num: 49504
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5272
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8550
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.440922190201729e-3
allele num: 694
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 3.076923076923077e-4
allele num: 6500
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 4.00427122263748e-4
allele num: 7492
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.581501137225171e-5
allele num: 13190
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.59e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.55e-1

QD
type: SiteQuality
SIO_000300: 1.8e0

MQRankSum
type: SiteQuality
SIO_000300: 1.05e-1

DP
type: SiteQuality
SIO_000300: 2.56379e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.45e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.591e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.46e-1

GenotypeQuality
all individuals: 1298
bin: 9.25e1
variant carriers: 13

GenotypeQuality
all individuals: 1991
bin: 5.75e1
variant carriers: 40

GenotypeQuality
all individuals: 2883
bin: 7.5e0
variant carriers: 176

GenotypeQuality
all individuals: 1944
bin: 5.25e1
variant carriers: 41

GenotypeQuality
all individuals: 2283
bin: 4.75e1
variant carriers: 33

GenotypeQuality
all individuals: 2744
bin: 1.25e1
variant carriers: 158

GenotypeQuality
all individuals: 15893
bin: 9.75e1
variant carriers: 46

GenotypeQuality
all individuals: 6738
bin: 2.5e0
variant carriers: 130

GenotypeQuality
all individuals: 2320
bin: 4.25e1
variant carriers: 56

GenotypeQuality
all individuals: 1496
bin: 8.25e1
variant carriers: 17

GenotypeQuality
all individuals: 2374
bin: 3.75e1
variant carriers: 71

GenotypeQuality
all individuals: 2500
bin: 2.75e1
variant carriers: 67

GenotypeQuality
all individuals: 1774
bin: 6.75e1
variant carriers: 29

African
type: Population
allele count: 47
allele frequency: 6.273358248798718e-3
allele num: 7492
num of homozygotes: 0

Latino
type: Population
allele count: 74
allele frequency: 8.654970760233919e-3
allele num: 8550
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 23
allele frequency: 4.362670713201821e-3
allele num: 5272
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.440922190201729e-3
allele num: 694
num of homozygotes: 0

East Asian
type: Population
allele count: 49
allele frequency: 7.538461538461538e-3
allele num: 6500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 389
allele frequency: 7.857950872656755e-3
allele num: 49504
num of homozygotes: 0

South Asian
type: Population
allele count: 88
allele frequency: 6.67172100075815e-3
allele num: 13190
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.46e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.59e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.55e-1

QD
type: SiteQuality
SIO_000300: 1.8e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.591e-1

DP
type: SiteQuality
SIO_000300: 2.56379e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.45e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.05e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 1.010019392372333e-4
allele num: 49504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7492
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.169590643274854e-4
allele num: 8550
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.8e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

DP
type: SiteQuality
SIO_000300: 2.56379e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.45e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.591e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.46e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.59e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.55e-1

GenotypeQuality
all individuals: 2293
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2416
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1707
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1185
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2689
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 830
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31044
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7798
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 261
bin: 7.5e0
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11444
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.529145513487063e-5
allele num: 65396
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9928
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8348
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 7.86e-1

QD
type: SiteQuality
SIO_000300: 1.223e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.942e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.04e-1

DP
type: SiteQuality
SIO_000300: 2.032584e6

VQSLOD
type: SiteQuality
SIO_000300: 7.18e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeQuality
all individuals: 421
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2403
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 394
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GenotypeQuality
all individuals: 9114
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
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variant carriers: 0

GenotypeQuality
all individuals: 226
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GenotypeQuality
all individuals: 7796
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GenotypeQuality
all individuals: 30494
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1180
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8280
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9920
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65166
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16454
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -3.68e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.972e1

VQSLOD
type: SiteQuality
SIO_000300: -2.721e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.17e0

MQRankSum
type: SiteQuality
SIO_000300: 9.15e-1

DP
type: SiteQuality
SIO_000300: 2.021091e6

MQ
type: SiteQuality
SIO_000300: 5.826e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.98e-1

GenotypeQuality
all individuals: 260
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1328
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 962
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3650
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2207
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7383
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 132
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20505
bin: 6.25e1
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GenotypeQuality
all individuals: 2046
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variant carriers: 0

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

GenotypeQuality
all individuals: 1064
bin: 7.5e0
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.592103168285305e-5
allele num: 62810
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11180
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7934
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16322
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9530
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

DP
type: SiteQuality
SIO_000300: 1.766416e6

VQSLOD
type: SiteQuality
SIO_000300: -1.076e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.69e0

MQ
type: SiteQuality
SIO_000300: 6.051e1

QD
type: SiteQuality
SIO_000300: 1.753e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.75e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

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

Latino
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East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.624167614097775e-5
allele num: 61570
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BaseQRankSum
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VQSLOD
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FS
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MQ
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QD
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DP
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.62216526619732e-5
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ClippingRankSum
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MQRankSum
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MQ
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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DP
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FS
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6510
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 6.187353050365054e-5
allele num: 16162
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
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FS
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SIO_000300: 0.0e0

DP
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QD
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MQ
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 8946
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 4
allele frequency: 6.726985301537116e-5
allele num: 59462
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South Asian
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.16e-1

MQRankSum
type: SiteQuality
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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DP
type: SiteQuality
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InbreedingCoeff
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.411e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 1
allele frequency: 1.354279523293608e-4
allele num: 7384
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European (Non-Finnish)
type: Population
allele count: 42
allele frequency: 7.210795591113553e-4
allele num: 58246
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.364066193853428e-3
allele num: 846
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 60
allele frequency: 9.31098696461825e-3
allele num: 6444
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
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DP
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QD
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MQ
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VQSLOD
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.08e-1

ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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South Asian
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allele frequency: 6.068697657482704e-5
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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European (Non-Finnish)
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Latino
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African
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VQSLOD
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MQ
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InbreedingCoeff
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QD
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FS
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ClippingRankSum
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BaseQRankSum
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DP
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MQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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South Asian
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African
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European (Finnish)
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East Asian
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Latino
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European (Non-Finnish)
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FS
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MQ
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QD
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BaseQRankSum
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MQRankSum
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VQSLOD
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DP
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele num: 6584
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Latino
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East Asian
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South Asian
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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allele num: 906
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African
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MQ
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
type: SiteQuality
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MQRankSum
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ClippingRankSum
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QD
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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Other
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European (Non-Finnish)
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allele frequency: 0.0e0
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African
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South Asian
type: Population
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Latino
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allele frequency: 1.734906315058987e-4
allele num: 11528
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
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FS
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InbreedingCoeff
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ClippingRankSum
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MQ
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VQSLOD
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SIO_000300: -1.333e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.09e-1

DP
type: SiteQuality
SIO_000300: 1.916514e6

MQRankSum
type: SiteQuality
SIO_000300: 6.69e-1

QD
type: SiteQuality
SIO_000300: 9.59e0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.213739531496541e-4
allele num: 16478
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: 10372
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66462
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.07e-1

DP
type: SiteQuality
SIO_000300: 1.917201e6

QD
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SIO_000300: 9.17e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 8.1e-2

MQRankSum
type: SiteQuality
SIO_000300: -5.17e-1

FS
type: SiteQuality
SIO_000300: 6.09e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.82e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3008
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GenotypeQuality
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bin: 9.25e1
variant carriers: 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: 11522
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.009238361770636e-5
allele num: 66462
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.917201e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 9.17e0

FS
type: SiteQuality
SIO_000300: 6.09e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.07e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.17e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.76e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.1e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 577
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GenotypeQuality
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variant carriers: 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: 11526
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.157139551029854e-4
allele num: 8642
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66466
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.067961165048543e-5
allele num: 16480
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.49e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e0

MQRankSum
type: SiteQuality
SIO_000300: -1.878e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.84e0

DP
type: SiteQuality
SIO_000300: 1.918122e6

VQSLOD
type: SiteQuality
SIO_000300: 1.29e0

MQ
type: SiteQuality
SIO_000300: 5.414e1

QD
type: SiteQuality
SIO_000300: 7.62e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 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: 10372
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66468
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.735207357279195e-4
allele num: 11526
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.919004e6

QD
type: SiteQuality
SIO_000300: 1.285e1

MQ
type: SiteQuality
SIO_000300: 5.931e1

FS
type: SiteQuality
SIO_000300: 6.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.164e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

MQRankSum
type: SiteQuality
SIO_000300: -1.007e0

VQSLOD
type: SiteQuality
SIO_000300: 9.68e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4
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GenotypeQuality
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variant carriers: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.511956685215822e-5
allele num: 66490
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.094e1

FS
type: SiteQuality
SIO_000300: 5.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.44e-1

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.48e0

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.92347e6

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

MQ
type: SiteQuality
SIO_000300: 5.934e1

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66504
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156871818602499e-4
allele num: 8644
num of homozygotes: 0

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

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
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InbreedingCoeff
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FS
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
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DP
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MQRankSum
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66496
num of homozygotes: 0

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

Latino
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allele count: 1
allele frequency: 8.679048776254123e-5
allele num: 11522
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.637625289128758e-5
allele num: 10376
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
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East Asian
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DP
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
allele count: 0
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allele num: 906
num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 1.213444970270598e-4
allele num: 16482
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66496
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East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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Latino
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European (Finnish)
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allele count: 0
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MQRankSum
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
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QD
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ReadPosRankSum
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ClippingRankSum
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FS
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VQSLOD
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MQ
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11494
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505706628120577e-5
allele num: 66414
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10360
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16460
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.96e1

FS
type: SiteQuality
SIO_000300: 2.785e0

QD
type: SiteQuality
SIO_000300: 1.355e1

VQSLOD
type: SiteQuality
SIO_000300: 7.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.36e0

DP
type: SiteQuality
SIO_000300: 1.921937e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.19e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.54e-1

GenotypeQuality
all individuals: 46
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 23
bin: 7.5e0
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 773
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2453
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2420
bin: 9.75e1
variant carriers: 9

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.548992964338557e-5
allele num: 66234
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16432
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11470
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10328
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.086427267194157e-4
allele num: 6572
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.91e0

FS
type: SiteQuality
SIO_000300: 4.052e0

DP
type: SiteQuality
SIO_000300: 1.912883e6

QD
type: SiteQuality
SIO_000300: 1.238e1

MQRankSum
type: SiteQuality
SIO_000300: 5.669999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.071e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.55e-1

GenotypeQuality
all individuals: 155
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1566
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2428
bin: 9.75e1
variant carriers: 21

GenotypeQuality
all individuals: 47
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10322
num of homozygotes: 0

Latino
type: Population
allele count: 19
allele frequency: 1.658230057601676e-3
allele num: 11458
num of homozygotes: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16420
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.022791850553171e-5
allele num: 66164
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.212389380530973e-3
allele num: 904
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.025e0

DP
type: SiteQuality
SIO_000300: 1.907784e6

MQ
type: SiteQuality
SIO_000300: 5.153e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.72e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.48e0

FS
type: SiteQuality
SIO_000300: 1.564e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.5e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.543e0

QD
type: SiteQuality
SIO_000300: 8.949999999999999e0

GenotypeQuality
all individuals: 271
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 81
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 193
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2849
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variant carriers: 0

GenotypeQuality
all individuals: 770
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10312
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515886490419597e-5
allele num: 65968
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16364
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.917e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.06e0

DP
type: SiteQuality
SIO_000300: 1.896017e6

VQSLOD
type: SiteQuality
SIO_000300: 1.84e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.69e-1

QD
type: SiteQuality
SIO_000300: 1.245e1

GenotypeQuality
all individuals: 117
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35802
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2289
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variant carriers: 0

GenotypeQuality
all individuals: 2736
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variant carriers: 0

GenotypeQuality
all individuals: 545
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variant carriers: 0

GenotypeQuality
all individuals: 2397
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 8
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1582
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.053714844107857e-5
allele num: 65494
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16224
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11340
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10268
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.47e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

DP
type: SiteQuality
SIO_000300: 1.866909e6

MQRankSum
type: SiteQuality
SIO_000300: 5.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.53e0

QD
type: SiteQuality
SIO_000300: 8.9e0

FS
type: SiteQuality
SIO_000300: 1.97e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.91e-1

GenotypeQuality
all individuals: 545
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 54
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 81
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 429
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 51
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GenotypeQuality
all individuals: 760
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11340
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10268
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16224
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65494
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.166044776119403e-4
allele num: 8576
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.53e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.91e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.47e-1

FS
type: SiteQuality
SIO_000300: 1.97e0

DP
type: SiteQuality
SIO_000300: 1.866909e6

MQRankSum
type: SiteQuality
SIO_000300: 5.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

QD
type: SiteQuality
SIO_000300: 8.9e0

GenotypeQuality
all individuals: 82
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2392
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GenotypeQuality
all individuals: 10
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GenotypeQuality
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GenotypeQuality
all individuals: 62
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 5219
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GenotypeQuality
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GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 2268
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16166
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65124
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.767532721234616e-5
allele num: 10238
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6534
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11288
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.98e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.34e0

MQRankSum
type: SiteQuality
SIO_000300: 1.74e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.72e-1

FS
type: SiteQuality
SIO_000300: 2.61e0

VQSLOD
type: SiteQuality
SIO_000300: 8.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.139e0

DP
type: SiteQuality
SIO_000300: 1.848207e6

QD
type: SiteQuality
SIO_000300: 1.432e1

GenotypeQuality
all individuals: 16
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 886
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 4.25e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
all individuals: 2390
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 8685
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variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8486
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6520
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16066
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10190
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11164
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.550195324610901e-5
allele num: 64508
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.69e-1

DP
type: SiteQuality
SIO_000300: 1.820303e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.959e0

VQSLOD
type: SiteQuality
SIO_000300: -4.151e-1

FS
type: SiteQuality
SIO_000300: 5.244e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

MQ
type: SiteQuality
SIO_000300: 5.964e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

QD
type: SiteQuality
SIO_000300: 7.53e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.55e-1

GenotypeQuality
all individuals: 374
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2011
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 65
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 538
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variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8146
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46036
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 702
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.349527665317139e-4
allele num: 7410
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5142
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5862
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13268
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.933e0

MQ
type: SiteQuality
SIO_000300: 5.903e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.29e-2

DP
type: SiteQuality
SIO_000300: 1.111015e6

QD
type: SiteQuality
SIO_000300: 6.16e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.48e0

MQRankSum
type: SiteQuality
SIO_000300: 1.56e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.255e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.5e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1739
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GenotypeQuality
all individuals: 703
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variant carriers: 0

GenotypeQuality
all individuals: 530
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 540
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variant carriers: 0

GenotypeQuality
all individuals: 2010
bin: 9.75e1
variant carriers: 3

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1137
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7034
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12170
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5986
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 588
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.370569280343717e-5
allele num: 37240
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4062
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.659574468085106e-4
allele num: 3760
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.16e-2

QD
type: SiteQuality
SIO_000300: 1.248e1

MQRankSum
type: SiteQuality
SIO_000300: -3.5e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 9.00859e5

VQSLOD
type: SiteQuality
SIO_000300: 4.7e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.02e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.88e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.01e-1

GenotypeQuality
all individuals: 14753
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5259
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 3.75e1
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GenotypeQuality
all individuals: 61
bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
all individuals: 2014
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 521
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3010
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2376
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 3.400204012240735e-4
allele num: 5882
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 496
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.885369532428356e-4
allele num: 5304
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11266
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 1.30718954248366e-4
allele num: 30600
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.9e-2

DP
type: SiteQuality
SIO_000300: 7.88266e5

MQRankSum
type: SiteQuality
SIO_000300: -3.9e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.33e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.67e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.88e-2

QD
type: SiteQuality
SIO_000300: 1.649e1

VQSLOD
type: SiteQuality
SIO_000300: 7.6e-1

GenotypeQuality
all individuals: 2007
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 74
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1818
bin: 2.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 826
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1453
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5894
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 496
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2390
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.265626020508131e-5
allele num: 30622
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11260
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3012
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5288
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.88e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.52e0

DP
type: SiteQuality
SIO_000300: 7.87233e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.7e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.926e0

MQRankSum
type: SiteQuality
SIO_000300: -6.78e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.022e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.7e-2

GenotypeQuality
all individuals: 1504
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4284
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 1178
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variant carriers: 0

GenotypeQuality
all individuals: 522
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variant carriers: 0

GenotypeQuality
all individuals: 16705
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2006
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 821
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 732
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 26664
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10734
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4928
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4944
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 478
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1806
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.31e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

QD
type: SiteQuality
SIO_000300: 6.06e0

MQ
type: SiteQuality
SIO_000300: 5.79e1

DP
type: SiteQuality
SIO_000300: 7.33062e5

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.002e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.76e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.307e0

GenotypeQuality
all individuals: 1264
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 703
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1869
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2806
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
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variant carriers: 0

GenotypeQuality
all individuals: 17721
bin: 7.5e0
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GenotypeQuality
all individuals: 526
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variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2005
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3720
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4444
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1360
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22354
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10196
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 422
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2126
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 6.84014e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.76e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.017e0

QD
type: SiteQuality
SIO_000300: 7.22e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -4.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.21e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.505e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.64e0

GenotypeQuality
all individuals: 524
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1757
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2608
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 921
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1727
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 5.25e1
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GenotypeQuality
all individuals: 2585
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 790
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2004
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 318
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1188
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1124
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.121901249743905e-5
allele num: 19524
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2916
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 374
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1906
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4072
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9782
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.51e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.989e1

DP
type: SiteQuality
SIO_000300: 6.49685e5

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.07e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.14e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 6.33e-1

QD
type: SiteQuality
SIO_000300: 1.589e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.33e-1

GenotypeQuality
all individuals: 450
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 251
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2881
bin: 9.75e1
variant carriers: 125

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 1

GenotypeQuality
all individuals: 423
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variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 458
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 963
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 246
bin: 7.25e1
variant carriers: 1

African
type: Population
allele count: 51
allele frequency: 9.107142857142857e-2
allele num: 560
num of homozygotes: 4

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 49
allele frequency: 1.35284373274434e-2
allele num: 3622
num of homozygotes: 0

South Asian
type: Population
allele count: 29
allele frequency: 3.805774278215223e-3
allele num: 7620
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 7.575757575757576e-3
allele num: 132
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.97e0

FS
type: SiteQuality
SIO_000300: 2.262e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.332e0

DP
type: SiteQuality
SIO_000300: 2.54444e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.83e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.16e-1

MQ
type: SiteQuality
SIO_000300: 5.987e1

QD
type: SiteQuality
SIO_000300: 1.381e1

GenotypeQuality
all individuals: 42
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 349
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GenotypeQuality
all individuals: 426
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GenotypeQuality
all individuals: 251
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GenotypeQuality
all individuals: 464
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variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.25e1
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GenotypeQuality
all individuals: 997
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 450
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 558
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.521811154058532e-4
allele num: 3622
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.624671916010499e-4
allele num: 7620
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.71e-2

FS
type: SiteQuality
SIO_000300: 1.1133e1

QD
type: SiteQuality
SIO_000300: 1.299e1

MQRankSum
type: SiteQuality
SIO_000300: 9.86e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.122e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.3e0

DP
type: SiteQuality
SIO_000300: 2.48924e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.15e-1

GenotypeQuality
all individuals: 67
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1014
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2810
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 420
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GenotypeQuality
all individuals: 464
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GenotypeQuality
all individuals: 1678
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 451
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variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 558
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.937007874015748e-4
allele num: 7620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3622
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.69e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 8.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.91e-1

QD
type: SiteQuality
SIO_000300: 1.487e1

DP
type: SiteQuality
SIO_000300: 2.48747e5

FS
type: SiteQuality
SIO_000300: 8.896000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.1e-2

MQRankSum
type: SiteQuality
SIO_000300: -5.71e-1

MQ
type: SiteQuality
SIO_000300: 5.719e1

GenotypeQuality
all individuals: 179
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 3.25e1
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GenotypeQuality
all individuals: 1733
bin: 7.5e0
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GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3614
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

South Asian
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allele frequency: 1.312335958005249e-4
allele num: 7620
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 558
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.68e-1

FS
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.42e-2

MQRankSum
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SIO_000300: 1.39e0

QD
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ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 6.018e1

VQSLOD
type: SiteQuality
SIO_000300: 9.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.1e-2

DP
type: SiteQuality
SIO_000300: 2.48297e5

GenotypeQuality
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variant carriers: 1

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

Latino
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allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.792114695340502e-3
allele num: 558
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7620
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3610
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.74e-2

VQSLOD
type: SiteQuality
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QD
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BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 6.641e0

MQRankSum
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SIO_000300: -3.22e-1

DP
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SIO_000300: 2.48164e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ReadPosRankSum
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SIO_000300: 1.04e0

GenotypeQuality
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.915708812260536e-3
allele num: 522
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7606
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 180
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3554
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.236e0

QD
type: SiteQuality
SIO_000300: 2.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.73e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.337e0

BaseQRankSum
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SIO_000300: -2.369e0

MQRankSum
type: SiteQuality
SIO_000300: 1.58e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.68e0

DP
type: SiteQuality
SIO_000300: 2.46263e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3534
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 180
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 1.314751511964239e-4
allele num: 7606
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 510
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.75e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.18e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.963e0

VQSLOD
type: SiteQuality
SIO_000300: -8.24e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.71e-1

DP
type: SiteQuality
SIO_000300: 2.4591e5

BaseQRankSum
type: SiteQuality
SIO_000300: 4.37e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.47e-1

QD
type: SiteQuality
SIO_000300: 1.081e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 1

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

South Asian
type: Population
allele count: 1
allele frequency: 1.321003963011889e-4
allele num: 7570
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 170
num of homozygotes: 0

African
type: Population
allele count: 34
allele frequency: 8.45771144278607e-2
allele num: 402
num of homozygotes: 3

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 3.638568829593693e-3
allele num: 3298
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 130
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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QD
type: SiteQuality
SIO_000300: 1.65e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.86e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.4e-2

BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.7e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.38313e5

VQSLOD
type: SiteQuality
SIO_000300: 5.46e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16398
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9294
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.135189365437672e-5
allele num: 63792
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8444
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11406
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.682e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.13e-1

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
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DP
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SIO_000300: 2.318333e6

QD
type: SiteQuality
SIO_000300: 8.109999999999999e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63764
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16400
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African
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allele count: 1
allele frequency: 1.078981441519206e-4
allele num: 9268
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
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BaseQRankSum
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SIO_000300: -1.866e0

FS
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VQSLOD
type: SiteQuality
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ClippingRankSum
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DP
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InbreedingCoeff
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MQRankSum
type: SiteQuality
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MQ
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8444
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63792
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Other
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South Asian
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Latino
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allele frequency: 3.506311360448808e-4
allele num: 11408
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African
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.25e-1

MQRankSum
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
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DP
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VQSLOD
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ReadPosRankSum
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QD
type: SiteQuality
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FS
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MQ
type: SiteQuality
SIO_000300: 5.974e1

GenotypeQuality
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variant carriers: 2

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

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

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

European (Non-Finnish)
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East Asian
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Other
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MQRankSum
type: SiteQuality
SIO_000300: 1.91e-1

FS
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InbreedingCoeff
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MQ
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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DP
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QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7510
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1824
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15400
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 81
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11420
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63868
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.075500107550011e-4
allele num: 9298
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16406
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 4.41e-1

DP
type: SiteQuality
SIO_000300: 2.332887e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 7.24e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.5e-2

FS
type: SiteQuality
SIO_000300: 6.830000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.257e1

MQ
type: SiteQuality
SIO_000300: 5.881e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.28e0

GenotypeQuality
all individuals: 318
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29492
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7510
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 2.5e0
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15400
bin: 9.75e1
variant carriers: 4

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 670
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1625
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11420
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.697187950147179e-5
allele num: 63868
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.095330976472023e-5
allele num: 16406
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9298
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.28e0

MQRankSum
type: SiteQuality
SIO_000300: 4.41e-1

FS
type: SiteQuality
SIO_000300: 6.830000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

DP
type: SiteQuality
SIO_000300: 2.332887e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.5e-2

MQ
type: SiteQuality
SIO_000300: 5.881e1

QD
type: SiteQuality
SIO_000300: 1.257e1

GenotypeQuality
all individuals: 671
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1935
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 468
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15398
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 318
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variant carriers: 0

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 1.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16408
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11420
num of homozygotes: 0

East Asian
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: 878
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.562939576755963e-5
allele num: 63982
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9324
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.28e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.143e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

FS
type: SiteQuality
SIO_000300: 1.142e0

VQSLOD
type: SiteQuality
SIO_000300: 5.590000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e0

QD
type: SiteQuality
SIO_000300: 1.082e1

DP
type: SiteQuality
SIO_000300: 2.334764e6

MQ
type: SiteQuality
SIO_000300: 5.929e1

GenotypeQuality
all individuals: 1914
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 65
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 511
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variant carriers: 0

GenotypeQuality
all individuals: 15398
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1631
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 94
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variant carriers: 0

GenotypeQuality
all individuals: 29751
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 469
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9326
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63982
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16408
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11416
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -3.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -5.72e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.856e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 8.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.72e-1

MQ
type: SiteQuality
SIO_000300: 6.236e1

VQSLOD
type: SiteQuality
SIO_000300: 5.37e0

DP
type: SiteQuality
SIO_000300: 2.335261e6

GenotypeQuality
all individuals: 58
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7577
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15399
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 58
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 672
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1466
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 468
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1963
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63984
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.752234098475556e-4
allele num: 11414
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9338
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16408
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8440
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.58e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.46e-1

FS
type: SiteQuality
SIO_000300: 4.977e0

QD
type: SiteQuality
SIO_000300: 1.166e1

MQRankSum
type: SiteQuality
SIO_000300: -2.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.29e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.58e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

DP
type: SiteQuality
SIO_000300: 2.336639e6

GenotypeQuality
all individuals: 29795
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1631
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 672
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15399
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 468
bin: 9.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63984
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16408
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.369668246445498e-4
allele num: 8440
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9338
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.46e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.58e-1

DP
type: SiteQuality
SIO_000300: 2.336639e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.29e0

VQSLOD
type: SiteQuality
SIO_000300: 1.58e0

MQRankSum
type: SiteQuality
SIO_000300: -2.37e-1

QD
type: SiteQuality
SIO_000300: 1.166e1

FS
type: SiteQuality
SIO_000300: 4.977e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

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

GenotypeQuality
all individuals: 15395
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 70
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1987
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 671
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 30
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29977
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7584
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1466
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.762705923589205e-5
allele num: 11412
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8448
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16414
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

African
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: 64032
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.120000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.8e-1

DP
type: SiteQuality
SIO_000300: 2.337857e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.031e1

FS
type: SiteQuality
SIO_000300: 5.645e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.91e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 6.4e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.81e-1

GenotypeQuality
all individuals: 444
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7600
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1633
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15393
bin: 9.75e1
variant carriers: 1