2-74595247-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595247
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595247
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 45714
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1464C>G
  hgvsp: ENSP00000387270.1:p.Ile488Met
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.2683C>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1755C>G
  hgvsp: ENSP00000416711.1:p.Ile585Met
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1755C>G
  hgvsp: ENSP00000386406.1:p.Ile585Met
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+1180C>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1815C>G
  hgvsp: ENSP00000387327.1:p.Ile605Met
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1464C>G
  hgvsp: ENSP00000384844.2:p.Ile488Met
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1806C>G
  hgvsp: ENSP00000386843.3:p.Ile602Met
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1845C>G
  hgvsp: ENSP00000377571.3:p.Ile615Met
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1866C>G
  hgvsp: ENSP00000354791.3:p.Ile622Met
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10089
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11649
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27025
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 701
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ile622Met
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

2-74595257-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595257
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595257
    reference: chr 2
allele count: 1
allele frequency: 2.413243882426758e-5
allele num: 41438
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1856C>T
  hgvsp: ENSP00000354791.3:p.Ala619Val
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.2673C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1745C>T
  hgvsp: ENSP00000416711.1:p.Ala582Val
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1835C>T
  hgvsp: ENSP00000377571.3:p.Ala612Val
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1805C>T
  hgvsp: ENSP00000387327.1:p.Ala602Val
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1796C>T
  hgvsp: ENSP00000386843.3:p.Ala599Val
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+1170C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1745C>T
  hgvsp: ENSP00000386406.1:p.Ala582Val
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1454C>T
  hgvsp: ENSP00000384844.2:p.Ala485Val
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1454C>T
  hgvsp: ENSP00000387270.1:p.Ala485Val
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12970
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10330
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26250
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala619Val
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

http://identifiers.org/exac.variant/2-74595258-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595258
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595258
    reference: chr 2
allele count: 1
allele frequency: 2.433208428633997e-5
allele num: 41098
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1855G>T
  hgvsp: ENSP00000354791.3:p.Ala619Ser
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1804G>T
  hgvsp: ENSP00000387327.1:p.Ala602Ser
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1795G>T
  hgvsp: ENSP00000386843.3:p.Ala599Ser
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1834G>T
  hgvsp: ENSP00000377571.3:p.Ala612Ser
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1744G>T
  hgvsp: ENSP00000416711.1:p.Ala582Ser
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1744G>T
  hgvsp: ENSP00000386406.1:p.Ala582Ser
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+1169G>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.2672G>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1453G>T
  hgvsp: ENSP00000387270.1:p.Ala485Ser
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1453G>T
  hgvsp: ENSP00000384844.2:p.Ala485Ser
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10205
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13278
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala619Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

2-74595276-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595276
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595276
    reference: chr 2
allele count: 1
allele frequency: 3.01295570955107e-5
allele num: 33190
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+1151T>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1834-18T>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.2654T>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1453-18T>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1744-18T>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1804-18T>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1744-18T>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1453-18T>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1795-18T>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1855-18T>C
  variant of: http://identifiers.org/hgnc/2711
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7439
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1327
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21692
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21143
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1650
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 848
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD

2-74595281-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595281
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595281
    reference: chr 2
allele count: 1
allele frequency: 3.182686187141948e-5
allele num: 31420
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1453-23G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+1146G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1744-23G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1804-23G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.2649G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1744-23G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1855-23G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1795-23G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1834-23G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1453-23G>A
  variant of: http://identifiers.org/hgnc/2711
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20549
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22958
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6653
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1054
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22992
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum

2-74595297-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595297
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595297
    reference: chr 2
allele count: 1
allele frequency: 3.833180006133088e-5
allele num: 26088
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1795-39C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1744-39C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1855-39C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1453-39C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1744-39C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+1130C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1804-39C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.2633C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1834-39C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1453-39C>T
  variant of: http://identifiers.org/hgnc/2711
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4250
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26057
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18783
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1305
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5932
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 7.25e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD

2-74595299-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595299
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595299
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 25806
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1744-41C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+1128C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1795-41C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1744-41C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1855-41C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1804-41C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.2631C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1834-41C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1453-41C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1453-41C>T
  variant of: http://identifiers.org/hgnc/2711
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26078
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18845
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9446
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1472
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

2-74595304-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595304
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595304
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 24334
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1804-46C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+1123C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1744-46C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1744-46C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1453-46C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1795-46C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1834-46C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1453-46C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.2626C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1855-46C>T
  variant of: http://identifiers.org/hgnc/2711
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19192
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25972
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3443
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1084
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6801
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 556
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: East Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

2-74595309-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595309
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595309
    reference: chr 2
allele count: 1
allele frequency: 4.244121891180715e-5
allele num: 23562
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1453-51G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1453-51G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1795-51G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1744-51G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1855-51G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.2621G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1804-51G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1744-51G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+1118G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1834-51G>A
  variant of: http://identifiers.org/hgnc/2711
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19231
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26053
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3261
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 905
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22333
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/2-74595810-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595810
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595810
    reference: chr 2
allele count: 1
allele frequency: 8.249191579225235e-6
allele num: 121224
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1794+45G>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1833+45G>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1743+45G>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.2120G>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1452+45G>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1452+45G>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1743+45G>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+617G>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1803+45G>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1854+45G>T
  variant of: http://identifiers.org/hgnc/2711
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19003
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9094
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2083
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11973
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3015
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5351
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 665
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD

2-74595810-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595810
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595810
    reference: chr 2
allele count: 22
allele frequency: 1.814822147429552e-4
allele num: 121224
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1803+45G>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1743+45G>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+617G>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1743+45G>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1794+45G>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.2120G>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1833+45G>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1452+45G>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1854+45G>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1452+45G>C
  variant of: http://identifiers.org/hgnc/2711
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2083
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11973
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5351
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9094
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19003
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3015
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13741
  bin: 9.75e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

2-74595810-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595810
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595810
    reference: chr 2
allele count: 1
allele frequency: 8.249191579225235e-6
allele num: 121224
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1803+45G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1452+45G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1452+45G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.2120G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1854+45G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1833+45G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1743+45G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1743+45G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1794+45G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+617G>A
  variant of: http://identifiers.org/hgnc/2711
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2083
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3015
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19003
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5351
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9094
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11973
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8645
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQ

2-74595815-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595815
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595815
    reference: chr 2
allele count: 1
allele frequency: 8.246742536698004e-6
allele num: 121260
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1833+40A>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+612A>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1452+40A>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1452+40A>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1743+40A>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1794+40A>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.2115A>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1743+40A>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1803+40A>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1854+40A>T
  variant of: http://identifiers.org/hgnc/2711
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3009
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9664
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11990
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19227
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5348
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8724
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQRankSum

2-74595817-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595817
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595817
    reference: chr 2
allele count: 1
allele frequency: 8.246742536698004e-6
allele num: 121260
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1833+38T>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1803+38T>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1452+38T>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1743+38T>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1854+38T>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.2113T>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+610T>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1794+38T>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1452+38T>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1743+38T>A
  variant of: http://identifiers.org/hgnc/2711
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9806
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3012
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19316
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12026
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5349
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3519
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/2-74595818-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595818
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595818
    reference: chr 2
allele count: 1
allele frequency: 8.246062505153789e-6
allele num: 121270
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1854+37G>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1794+37G>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1803+37G>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+609G>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1743+37G>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.2112G>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1743+37G>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1452+37G>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1452+37G>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1833+37G>T
  variant of: http://identifiers.org/hgnc/2711
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19347
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9872
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5352
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12039
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3014
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13727
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8728
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum

2-74595824-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595824
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595824
    reference: chr 2
allele count: 1
allele frequency: 8.244159013339049e-6
allele num: 121298
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1452+31A>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1833+31A>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1803+31A>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+603A>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1743+31A>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1854+31A>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1452+31A>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.2106A>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1794+31A>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1743+31A>G
  variant of: http://identifiers.org/hgnc/2711
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12045
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10128
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3012
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5350
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3180
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

2-74595828-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595828
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595828
    reference: chr 2
allele count: 3
allele frequency: 2.472758444470088e-5
allele num: 121322
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1803+27C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1833+27C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1452+27C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1794+27C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.2102C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1854+27C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+599C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1743+27C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1743+27C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1452+27C>T
  variant of: http://identifiers.org/hgnc/2711
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5347
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10158
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12073
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3016
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19552
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23322
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP

http://identifiers.org/exac.variant/2-74595832-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595832
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595832
    reference: chr 2
allele count: 1
allele frequency: 8.241169586787756e-6
allele num: 121342
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1833+23T>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1452+23T>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1803+23T>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1794+23T>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1854+23T>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1743+23T>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1743+23T>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1452+23T>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.2098T>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+595T>G
  variant of: http://identifiers.org/hgnc/2711
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12080
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10173
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3012
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5352
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19631
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

2-74595835-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595835
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595835
    reference: chr 2
allele count: 2
allele frequency: 1.648179585647652e-5
allele num: 121346
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.2095T>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1854+20T>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1803+20T>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1833+20T>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1743+20T>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+592T>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1794+20T>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1452+20T>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1452+20T>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1743+20T>C
  variant of: http://identifiers.org/hgnc/2711
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12080
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10168
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5352
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19636
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1581
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3016
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2082
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP

2-74595835-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595835
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595835
    reference: chr 2
allele count: 63
allele frequency: 5.191765694790104e-4
allele num: 121346
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1833+20T>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1743+20T>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1854+20T>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+592T>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1452+20T>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.2095T>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1743+20T>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1803+20T>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1452+20T>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1794+20T>A
  variant of: http://identifiers.org/hgnc/2711
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5352
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1581
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10168
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2082
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12080
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3016
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19636
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 5.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 3167
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 1
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

2-74595843-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595843
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595843
    reference: chr 2
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1743+12C>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1452+12C>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1794+12C>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1803+12C>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1833+12C>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1743+12C>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+584C>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1452+12C>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.2087C>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1854+12C>A
  variant of: http://identifiers.org/hgnc/2711
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19701
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5354
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10182
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2077
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12098
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3019
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4304
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

2-74595845-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595845
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595845
    reference: chr 2
allele count: 3
allele frequency: 2.471536142096851e-5
allele num: 121382
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1803+10A>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1833+10A>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1794+10A>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1452+10A>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1452+10A>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1743+10A>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1743+10A>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.2085A>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+582A>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1854+10A>G
  variant of: http://identifiers.org/hgnc/2711
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19706
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12101
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10185
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5353
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 1
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

2-74595859-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595859
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595859
    reference: chr 2
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1790G>A
  hgvsp: ENSP00000386843.3:p.Cys597Tyr
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.2071G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1799G>A
  hgvsp: ENSP00000387327.1:p.Cys600Tyr
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1448G>A
  hgvsp: ENSP00000387270.1:p.Cys483Tyr
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1739G>A
  hgvsp: ENSP00000416711.1:p.Cys580Tyr
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1448G>A
  hgvsp: ENSP00000384844.2:p.Cys483Tyr
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1829G>A
  hgvsp: ENSP00000377571.3:p.Cys610Tyr
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1739G>A
  hgvsp: ENSP00000386406.1:p.Cys580Tyr
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+568G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1850G>A
  hgvsp: ENSP00000354791.3:p.Cys617Tyr
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5353
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3020
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10171
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19744
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12102
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Cys617Tyr
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/2-74595861-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595861
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595861
    reference: chr 2
allele count: 2
allele frequency: 1.647446457990115e-5
allele num: 121400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1797T>G
  hgvsp: ENSP00000387327.1:p.Ile599Met
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1788T>G
  hgvsp: ENSP00000386843.3:p.Ile596Met
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+566T>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1737T>G
  hgvsp: ENSP00000386406.1:p.Ile579Met
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1446T>G
  hgvsp: ENSP00000384844.2:p.Ile482Met
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1737T>G
  hgvsp: ENSP00000416711.1:p.Ile579Met
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1848T>G
  hgvsp: ENSP00000354791.3:p.Ile616Met
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1446T>G
  hgvsp: ENSP00000387270.1:p.Ile482Met
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.2069T>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1827T>G
  hgvsp: ENSP00000377571.3:p.Ile609Met
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19746
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12103
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10172
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5352
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ile616Met
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP

2-74595872-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595872
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595872
    reference: chr 2
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1816C>T
  hgvsp: ENSP00000377571.3:p.Pro606Ser
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1435C>T
  hgvsp: ENSP00000384844.2:p.Pro479Ser
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1777C>T
  hgvsp: ENSP00000386843.3:p.Pro593Ser
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1435C>T
  hgvsp: ENSP00000387270.1:p.Pro479Ser
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1786C>T
  hgvsp: ENSP00000387327.1:p.Pro596Ser
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1726C>T
  hgvsp: ENSP00000416711.1:p.Pro576Ser
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.2058C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+555C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1837C>T
  hgvsp: ENSP00000354791.3:p.Pro613Ser
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1726C>T
  hgvsp: ENSP00000386406.1:p.Pro576Ser
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10173
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5352
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19755
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12101
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro613Ser
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

2-74595875-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595875
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595875
    reference: chr 2
allele count: 3
allele frequency: 2.471088267272907e-5
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1783A>T
  hgvsp: ENSP00000387327.1:p.Met595Leu
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1723A>T
  hgvsp: ENSP00000416711.1:p.Met575Leu
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+552A>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1723A>T
  hgvsp: ENSP00000386406.1:p.Met575Leu
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1432A>T
  hgvsp: ENSP00000387270.1:p.Met478Leu
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1834A>T
  hgvsp: ENSP00000354791.3:p.Met612Leu
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1774A>T
  hgvsp: ENSP00000386843.3:p.Met592Leu
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.2055A>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1432A>T
  hgvsp: ENSP00000384844.2:p.Met478Leu
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1813A>T
  hgvsp: ENSP00000377571.3:p.Met605Leu
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19757
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10175
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12099
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5351
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Met612Leu
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD

2-74595876-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595876
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595876
    reference: chr 2
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1722C>A
  hgvsp: ENST00000409240.1:c.1722C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1833C>A
  hgvsp: ENST00000361874.3:c.1833C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1431C>A
  hgvsp: ENST00000409438.1:c.1431C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1722C>A
  hgvsp: ENST00000434055.1:c.1722C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.2054C>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1812C>A
  hgvsp: ENST00000394003.3:c.1812C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+551C>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1773C>A
  hgvsp: ENST00000409567.3:c.1773C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1782C>A
  hgvsp: ENST00000409868.1:c.1782C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1431C>A
  hgvsp: ENST00000407639.2:c.1431C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10177
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5351
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19758
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12100
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1961
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu611Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

2-74595878-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595878
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595878
    reference: chr 2
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1831C>T
  hgvsp: ENSP00000354791.3:p.Leu611Phe
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1429C>T
  hgvsp: ENSP00000387270.1:p.Leu477Phe
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+549C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1771C>T
  hgvsp: ENSP00000386843.3:p.Leu591Phe
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1429C>T
  hgvsp: ENSP00000384844.2:p.Leu477Phe
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1780C>T
  hgvsp: ENSP00000387327.1:p.Leu594Phe
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1720C>T
  hgvsp: ENSP00000416711.1:p.Leu574Phe
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1720C>T
  hgvsp: ENSP00000386406.1:p.Leu574Phe
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.2052C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1810C>T
  hgvsp: ENSP00000377571.3:p.Leu604Phe
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3019
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19757
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12103
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10175
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5349
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu611Phe
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

2-74595887-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595887
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595887
    reference: chr 2
allele count: 12
allele frequency: 9.884190237714775e-5
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1711G>A
  hgvsp: ENSP00000416711.1:p.Val571Met
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.2043G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1420G>A
  hgvsp: ENSP00000384844.2:p.Val474Met
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1762G>A
  hgvsp: ENSP00000386843.3:p.Val588Met
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1771G>A
  hgvsp: ENSP00000387327.1:p.Val591Met
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1420G>A
  hgvsp: ENSP00000387270.1:p.Val474Met
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1801G>A
  hgvsp: ENSP00000377571.3:p.Val601Met
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+540G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1711G>A
  hgvsp: ENSP00000386406.1:p.Val571Met
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1822G>A
  hgvsp: ENSP00000354791.3:p.Val608Met
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19765
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10159
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5345
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12105
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val608Met
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum

2-74595893-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595893
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595893
    reference: chr 2
allele count: 2
allele frequency: 1.647337901950448e-5
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1765G>A
  hgvsp: ENSP00000387327.1:p.Val589Ile
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1705G>A
  hgvsp: ENSP00000416711.1:p.Val569Ile
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+534G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1414G>A
  hgvsp: ENSP00000384844.2:p.Val472Ile
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1756G>A
  hgvsp: ENSP00000386843.3:p.Val586Ile
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1414G>A
  hgvsp: ENSP00000387270.1:p.Val472Ile
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.2037G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1705G>A
  hgvsp: ENSP00000386406.1:p.Val569Ile
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1816G>A
  hgvsp: ENSP00000354791.3:p.Val606Ile
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1795G>A
  hgvsp: ENSP00000377571.3:p.Val599Ile
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12110
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19768
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5346
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10163
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1547
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Val606Ile
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

2-74595903-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595903
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595903
    reference: chr 2
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1746C>T
  hgvsp: ENST00000409567.3:c.1746C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1404C>T
  hgvsp: ENST00000407639.2:c.1404C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+524C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1806C>T
  hgvsp: ENST00000361874.3:c.1806C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1695C>T
  hgvsp: ENST00000434055.1:c.1695C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1404C>T
  hgvsp: ENST00000409438.1:c.1404C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1785C>T
  hgvsp: ENST00000394003.3:c.1785C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.2027C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1695C>T
  hgvsp: ENST00000409240.1:c.1695C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1755C>T
  hgvsp: ENST00000409868.1:c.1755C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5346
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10157
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12109
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19776
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asp602Asp
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

2-74595916-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595916
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595916
    reference: chr 2
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1682G>A
  hgvsp: ENSP00000416711.1:p.Arg561Gln
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.2014G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1742G>A
  hgvsp: ENSP00000387327.1:p.Arg581Gln
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1772G>A
  hgvsp: ENSP00000377571.3:p.Arg591Gln
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+511G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1793G>A
  hgvsp: ENSP00000354791.3:p.Arg598Gln
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1733G>A
  hgvsp: ENSP00000386843.3:p.Arg578Gln
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1391G>A
  hgvsp: ENSP00000384844.2:p.Arg464Gln
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1391G>A
  hgvsp: ENSP00000387270.1:p.Arg464Gln
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1682G>A
  hgvsp: ENSP00000386406.1:p.Arg561Gln
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3019
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10136
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5347
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12109
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19794
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg598Gln
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

2-74595917-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595917
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595917
    reference: chr 2
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1741C>T
  hgvsp: ENSP00000387327.1:p.Arg581Trp
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1732C>T
  hgvsp: ENSP00000386843.3:p.Arg578Trp
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+510C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1792C>T
  hgvsp: ENSP00000354791.3:p.Arg598Trp
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1681C>T
  hgvsp: ENSP00000386406.1:p.Arg561Trp
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1681C>T
  hgvsp: ENSP00000416711.1:p.Arg561Trp
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1390C>T
  hgvsp: ENSP00000384844.2:p.Arg464Trp
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.2013C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1390C>T
  hgvsp: ENSP00000387270.1:p.Arg464Trp
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1771C>T
  hgvsp: ENSP00000377571.3:p.Arg591Trp
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3019
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5348
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19793
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10134
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12111
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg598Trp
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum

2-74595934-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595934
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595934
    reference: chr 2
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1664T>A
  hgvsp: ENSP00000416711.1:p.Met555Lys
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1775T>A
  hgvsp: ENSP00000354791.3:p.Met592Lys
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1754T>A
  hgvsp: ENSP00000377571.3:p.Met585Lys
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1373T>A
  hgvsp: ENSP00000387270.1:p.Met458Lys
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1724T>A
  hgvsp: ENSP00000387327.1:p.Met575Lys
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+493T>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1715T>A
  hgvsp: ENSP00000386843.3:p.Met572Lys
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1664T>A
  hgvsp: ENSP00000386406.1:p.Met555Lys
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1373T>A
  hgvsp: ENSP00000384844.2:p.Met458Lys
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.1996T>A
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10124
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3020
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19803
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12110
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5347
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23628
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Met592Lys
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

2-74595935-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595935
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595935
    reference: chr 2
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1663A>G
  hgvsp: ENSP00000416711.1:p.Met555Val
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+492A>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1372A>G
  hgvsp: ENSP00000384844.2:p.Met458Val
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1753A>G
  hgvsp: ENSP00000377571.3:p.Met585Val
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1723A>G
  hgvsp: ENSP00000387327.1:p.Met575Val
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1714A>G
  hgvsp: ENSP00000386843.3:p.Met572Val
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.1995A>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1372A>G
  hgvsp: ENSP00000387270.1:p.Met458Val
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1663A>G
  hgvsp: ENSP00000386406.1:p.Met555Val
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1774A>G
  hgvsp: ENSP00000354791.3:p.Met592Val
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19805
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10123
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3020
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12111
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5344
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Met592Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP

2-74595939-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595939
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595939
    reference: chr 2
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1749C>T
  hgvsp: ENST00000394003.3:c.1749C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1719C>T
  hgvsp: ENST00000409868.1:c.1719C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.1991C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1659C>T
  hgvsp: ENST00000409240.1:c.1659C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1710C>T
  hgvsp: ENST00000409567.3:c.1710C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1659C>T
  hgvsp: ENST00000434055.1:c.1659C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1368C>T
  hgvsp: ENST00000409438.1:c.1368C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+488C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1368C>T
  hgvsp: ENST00000407639.2:c.1368C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1770C>T
  hgvsp: ENST00000361874.3:c.1770C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19801
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10120
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12112
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5344
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3020
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ala590Ala
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

2-74595948-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595948
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595948
    reference: chr 2
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1761G>C
  hgvsp: ENST00000361874.3:c.1761G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1650G>C
  hgvsp: ENST00000409240.1:c.1650G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1650G>C
  hgvsp: ENST00000434055.1:c.1650G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1359G>C
  hgvsp: ENST00000409438.1:c.1359G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1701G>C
  hgvsp: ENST00000409567.3:c.1701G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.1982G>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1740G>C
  hgvsp: ENST00000394003.3:c.1740G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1359G>C
  hgvsp: ENST00000407639.2:c.1359G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+479G>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1710G>C
  hgvsp: ENST00000409868.1:c.1710G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3020
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5345
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12113
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10113
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19799
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu587Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

2-74595951-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595951
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595951
    reference: chr 2
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1698C>T
  hgvsp: ENST00000409567.3:c.1698C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1647C>T
  hgvsp: ENST00000434055.1:c.1647C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1707C>T
  hgvsp: ENST00000409868.1:c.1707C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1356C>T
  hgvsp: ENST00000409438.1:c.1356C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.1979C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+476C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1737C>T
  hgvsp: ENST00000394003.3:c.1737C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1647C>T
  hgvsp: ENST00000409240.1:c.1647C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1356C>T
  hgvsp: ENST00000407639.2:c.1356C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1758C>T
  hgvsp: ENST00000361874.3:c.1758C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5343
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3021
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10099
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19806
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12115
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser586Ser
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP

2-74595961-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595961
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595961
    reference: chr 2
allele count: 2
allele frequency: 1.647555028337947e-5
allele num: 121392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1688G>A
  hgvsp: ENSP00000386843.3:p.Arg563Gln
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1346G>A
  hgvsp: ENSP00000384844.2:p.Arg449Gln
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1346G>A
  hgvsp: ENSP00000387270.1:p.Arg449Gln
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1727G>A
  hgvsp: ENSP00000377571.3:p.Arg576Gln
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1697G>A
  hgvsp: ENSP00000387327.1:p.Arg566Gln
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.1969G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1637G>A
  hgvsp: ENSP00000416711.1:p.Arg546Gln
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1748G>A
  hgvsp: ENSP00000354791.3:p.Arg583Gln
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+466G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1637G>A
  hgvsp: ENSP00000386406.1:p.Arg546Gln
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5344
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19793
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3021
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12120
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg583Gln
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ

2-74595972-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595972
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595972
    reference: chr 2
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1677C>T
  hgvsp: ENST00000409567.3:c.1677C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1335C>T
  hgvsp: ENST00000407639.2:c.1335C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+455C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1626C>T
  hgvsp: ENST00000434055.1:c.1626C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1686C>T
  hgvsp: ENST00000409868.1:c.1686C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1716C>T
  hgvsp: ENST00000394003.3:c.1716C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1626C>T
  hgvsp: ENST00000409240.1:c.1626C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.1958C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1737C>T
  hgvsp: ENST00000361874.3:c.1737C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1335C>T
  hgvsp: ENST00000409438.1:c.1335C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3019
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19799
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12119
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10049
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5346
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala579Ala
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD

2-74595981-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595981
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595981
    reference: chr 2
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1668G>A
  hgvsp: ENSP00000386843.3:p.Met556Ile
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1728G>A
  hgvsp: ENSP00000354791.3:p.Met576Ile
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.1949G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1617G>A
  hgvsp: ENSP00000416711.1:p.Met539Ile
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1326G>A
  hgvsp: ENSP00000384844.2:p.Met442Ile
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1326G>A
  hgvsp: ENSP00000387270.1:p.Met442Ile
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+446G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1617G>A
  hgvsp: ENSP00000386406.1:p.Met539Ile
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1707G>A
  hgvsp: ENSP00000377571.3:p.Met569Ile
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1677G>A
  hgvsp: ENSP00000387327.1:p.Met559Ile
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19811
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5339
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9984
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12111
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2073
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3553
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Met576Ile
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff

2-74595997-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74595997
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595997
    reference: chr 2
allele count: 1
allele frequency: 8.244838730954422e-6
allele num: 121288
alternate allele: G
annotation: Annotation
  canonical: false
  clinical significance: risk_factor
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.1933T>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  clinical significance: risk_factor
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1652T>C
  hgvsp: ENSP00000386843.3:p.Met551Thr
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  clinical significance: risk_factor
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1661T>C
  hgvsp: ENSP00000387327.1:p.Met554Thr
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  clinical significance: risk_factor
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1691T>C
  hgvsp: ENSP00000377571.3:p.Met564Thr
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  clinical significance: risk_factor
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1310T>C
  hgvsp: ENSP00000387270.1:p.Met437Thr
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  clinical significance: risk_factor
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1601T>C
  hgvsp: ENSP00000416711.1:p.Met534Thr
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  clinical significance: risk_factor
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1601T>C
  hgvsp: ENSP00000386406.1:p.Met534Thr
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  clinical significance: risk_factor
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1712T>C
  hgvsp: ENSP00000354791.3:p.Met571Thr
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  clinical significance: risk_factor
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+430T>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  clinical significance: risk_factor
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1310T>C
  hgvsp: ENSP00000384844.2:p.Met437Thr
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9836
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3021
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12095
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5329
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19785
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met571Thr
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: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/2-74596002-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74596002
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74596002
    reference: chr 2
allele count: 1
allele frequency: 8.245654540057389e-6
allele num: 121276
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.1928T>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1596T>G
  hgvsp: ENSP00000386406.1:p.Ile532Met
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1686T>G
  hgvsp: ENSP00000377571.3:p.Ile562Met
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1707T>G
  hgvsp: ENSP00000354791.3:p.Ile569Met
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1596T>G
  hgvsp: ENSP00000416711.1:p.Ile532Met
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1305T>G
  hgvsp: ENSP00000384844.2:p.Ile435Met
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+425T>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1305T>G
  hgvsp: ENSP00000387270.1:p.Ile435Met
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1656T>G
  hgvsp: ENSP00000387327.1:p.Ile552Met
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1647T>G
  hgvsp: ENSP00000386843.3:p.Ile549Met
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12077
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9765
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19748
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5326
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8714
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ile569Met
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

2-74596002-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74596002
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74596002
    reference: chr 2
allele count: 2
allele frequency: 1.649130908011478e-5
allele num: 121276
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1305T>C
  hgvsp: ENST00000407639.2:c.1305T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.1928T>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1647T>C
  hgvsp: ENST00000409567.3:c.1647T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+425T>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1656T>C
  hgvsp: ENST00000409868.1:c.1656T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1305T>C
  hgvsp: ENST00000409438.1:c.1305T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1686T>C
  hgvsp: ENST00000394003.3:c.1686T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1596T>C
  hgvsp: ENST00000434055.1:c.1596T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1596T>C
  hgvsp: ENST00000409240.1:c.1596T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1707T>C
  hgvsp: ENST00000361874.3:c.1707T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5326
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12077
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19748
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9765
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13692
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Ile569Ile
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

2-74596004-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74596004
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74596004
    reference: chr 2
allele count: 1
allele frequency: 8.246062505153789e-6
allele num: 121270
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1303A>G
  hgvsp: ENSP00000384844.2:p.Ile435Val
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1303A>G
  hgvsp: ENSP00000387270.1:p.Ile435Val
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1594A>G
  hgvsp: ENSP00000416711.1:p.Ile532Val
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1645A>G
  hgvsp: ENSP00000386843.3:p.Ile549Val
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+423A>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1594A>G
  hgvsp: ENSP00000386406.1:p.Ile532Val
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1654A>G
  hgvsp: ENSP00000387327.1:p.Ile552Val
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1705A>G
  hgvsp: ENSP00000354791.3:p.Ile569Val
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1684A>G
  hgvsp: ENSP00000377571.3:p.Ile562Val
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.1926A>G
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19729
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5326
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2071
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12071
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3020
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9740
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ile569Val
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

2-74596012-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74596012
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74596012
    reference: chr 2
allele count: 3
allele frequency: 2.475124993812188e-5
allele num: 121206
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1681-5C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1642-5C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1300-5C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.1923-5C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1702-5C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1591-5C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1591-5C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1651-5C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1300-5C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+415C>T
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12018
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3019
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5319
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19549
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9466
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2071
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 2.25e1
  variant carriers: 0
hgvs: c.1702-5C>T
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

2-74596014-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74596014
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74596014
    reference: chr 2
allele count: 16
allele frequency: 1.320349892721571e-4
allele num: 121180
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1681-7C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1702-7C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1300-7C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.1923-7C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+413C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1591-7C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1651-7C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1591-7C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1642-7C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1300-7C>T
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12001
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5315
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19494
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9378
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3140
  bin: 8.25e1
  variant carriers: 0
hgvs: c.1702-7C>T
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD

2-74596017-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74596017
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74596017
    reference: chr 2
allele count: 2
allele frequency: 1.651418568550385e-5
allele num: 121108
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1681-10C>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+410C>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1642-10C>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1651-10C>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1702-10C>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1300-10C>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1300-10C>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1591-10C>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.1923-10C>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1591-10C>G
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9235
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3019
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19310
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11952
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5311
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3135
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ

2-74596022-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74596022
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74596022
    reference: chr 2
allele count: 3
allele frequency: 2.477455158061639e-5
allele num: 121092
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+405C>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1591-15C>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1642-15C>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1651-15C>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1300-15C>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1300-15C>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1681-15C>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1702-15C>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1591-15C>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.1923-15C>G
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9119
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19185
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11876
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2070
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3008
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5302
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 631
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

2-74596024-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74596024
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74596024
    reference: chr 2
allele count: 1
allele frequency: 8.260912665631299e-6
allele num: 121052
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1642-17C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1591-17C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1681-17C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1651-17C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1300-17C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+403C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1591-17C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1300-17C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1702-17C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.1923-17C>T
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5289
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8982
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3003
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19080
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11827
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4158
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13668
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

2-74596026-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74596026
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74596026
    reference: chr 2
allele count: 5
allele frequency: 4.131070608258836e-5
allele num: 121034
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+401C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.1923-19C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1300-19C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1702-19C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1642-19C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1591-19C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1300-19C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1681-19C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1591-19C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1651-19C>T
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5275
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18940
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1414
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8836
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11785
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3003
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1927
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 786
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3100
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

2-74596027-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74596027
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74596027
    reference: chr 2
allele count: 2
allele frequency: 1.653083827880912e-5
allele num: 120986
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1591-20C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1651-20C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1300-20C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1642-20C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1681-20C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+400C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1591-20C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.1923-20C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1300-20C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1702-20C>T
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11757
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8709
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5270
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2997
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18801
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1520
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: G
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum

2-74596030-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74596030
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74596030
    reference: chr 2
allele count: 1
allele frequency: 8.268426187759421e-6
allele num: 120942
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1702-23C>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1591-23C>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1300-23C>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1651-23C>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+397C>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1591-23C>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.1923-23C>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1642-23C>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1300-23C>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1681-23C>A
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2993
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2064
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1749
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18416
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1818
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8363
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5248
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11626
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20314
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13663
  bin: 9.75e1
  variant carriers: 1
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: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

2-74596031-ACTCTTAGCCAGAGCTGAAAGAGCCCCAAAATT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74596031
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74595999
    reference: chr 2
allele count: 3
allele frequency: 2.480691947673938e-5
allele num: 120934
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 1573
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2990
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8167
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5235
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2212
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18157
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11526
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1077
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8053
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3335
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 974
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
reference allele: ACTCTTAGCCAGAGCTGAAAGAGCCCCAAAATT
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

2-74596034-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74596034
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74596034
    reference: chr 2
allele count: 1
allele frequency: 8.273214640280627e-6
allele num: 120872
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1651-27G>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1591-27G>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1702-27G>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1642-27G>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1681-27G>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+393G>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1300-27G>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1300-27G>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1591-27G>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.1923-27G>C
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7976
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2686
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2987
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11433
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17799
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5208
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2063
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1194
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3074
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum

2-74596040-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74596040
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74596040
    reference: chr 2
allele count: 1
allele frequency: 8.284317786430287e-6
allele num: 120710
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1642-33G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1591-33G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1300-33G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1300-33G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+387G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1681-33G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1651-33G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1702-33G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.1923-33G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1591-33G>A
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16169
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2058
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10746
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2972
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2592
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4857
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7643
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5152
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2014
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13656
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/2-74596045-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74596045
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74596045
    reference: chr 2
allele count: 1
allele frequency: 8.301097405076952e-6
allele num: 120466
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1651-38G>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1591-38G>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1300-38G>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.1923-38G>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1591-38G>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+382G>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1300-38G>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1642-38G>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1681-38G>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1702-38G>T
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14702
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4997
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2683
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2943
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6642
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9661
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8432
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1499
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2136
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

2-74596053-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74596053
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74596053
    reference: chr 2
allele count: 1
allele frequency: 8.322652595835345e-6
allele num: 120154
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1300-46C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+374C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1591-46C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1651-46C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1681-46C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1591-46C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1642-46C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1702-46C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1300-46C>T
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.1923-46C>T
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10713
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8910
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4920
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6923
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12878
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1817
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2851
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum

http://identifiers.org/exac.variant/2-74596058-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74596058
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74596058
    reference: chr 2
allele count: 1
allele frequency: 8.325562808045825e-6
allele num: 120112
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1642-51T>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1300-51T>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1591-51T>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1300-51T>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1591-51T>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1681-51T>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1702-51T>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.1923-51T>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1651-51T>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+369T>G
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2048
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6758
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8725
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11454
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4904
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2945
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12454
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1209
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD

2-74596058-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74596058
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74596058
    reference: chr 2
allele count: 1
allele frequency: 8.325562808045825e-6
allele num: 120112
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1300-51T>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1651-51T>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1642-51T>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1591-51T>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1702-51T>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.1923-51T>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1591-51T>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+369T>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1681-51T>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1300-51T>C
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12454
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2048
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2945
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11454
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8725
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6758
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4904
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1924
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1209
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

2-74596175-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74596175
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74596175
    reference: chr 2
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+252A>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1590+50A>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.1922+50A>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1299+50A>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1641+50A>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1650+50A>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1701+50A>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1299+50A>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1590+50A>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1680+50A>G
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6813
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5364
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3079
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3419
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4570
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5808
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7029
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2521
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3707
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4325
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3146
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4221
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum

2-74596177-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74596177
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74596177
    reference: chr 2
allele count: 2
allele frequency: 1.647609318878308e-5
allele num: 121388
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1650+48G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1299+48G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+250G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1641+48G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.1922+48G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1299+48G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1590+48G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1701+48G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1590+48G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1680+48G>A
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2521
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3078
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3420
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5808
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3706
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7029
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6813
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4331
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4570
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5363
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2706
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4224
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum

2-74596187-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74596187
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74596187
    reference: chr 2
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1650+38G>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1641+38G>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1299+38G>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1680+38G>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.1922+38G>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1701+38G>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+240G>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1299+38G>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1590+38G>C
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1590+38G>C
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7262
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2520
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6813
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4332
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4571
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7028
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5364
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3705
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3420
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5807
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQ

2-74596194-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74596194
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74596194
    reference: chr 2
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+233C>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1299+31C>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1650+31C>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1701+31C>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1590+31C>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1299+31C>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1680+31C>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1590+31C>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1641+31C>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.1922+31C>G
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5807
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4571
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7264
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5362
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6811
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4333
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3150
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7029
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2520
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3705
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3420
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3142
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2698
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP

2-74596198-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74596198
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74596198
    reference: chr 2
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1680+27A>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1641+27A>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.1922+27A>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1590+27A>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1590+27A>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+229A>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1299+27A>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1650+27A>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1701+27A>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1299+27A>G
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6816
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3143
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3421
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5366
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4347
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7028
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4571
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5806
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2520
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3704
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2515
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3140
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD

2-74596200-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74596200
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74596200
    reference: chr 2
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1590+25G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1299+25G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1590+25G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1650+25G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1701+25G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1299+25G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+227G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1680+25G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.1922+25G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1641+25G>A
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7029
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3159
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3421
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2520
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5360
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3704
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4343
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6812
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4571
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5807
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1611
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

2-74596207-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74596207
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74596207
    reference: chr 2
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1299+18G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1590+18G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1641+18G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1701+18G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1680+18G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1590+18G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1650+18G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.1922+18G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1299+18G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+220G>A
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7031
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5806
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4341
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4571
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3171
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2520
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6810
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3704
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3421
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5361
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7263
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

2-74596209-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74596209
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74596209
    reference: chr 2
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1590+16G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1680+16G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1701+16G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1299+16G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1650+16G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.1922+16G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1590+16G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1299+16G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1641+16G>A
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+218G>A
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2520
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4571
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4339
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3174
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3421
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5807
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6811
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5359
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7030
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3704
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41511
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3143
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/2-74596210-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74596210
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74596210
    reference: chr 2
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387327
  ensembl transcript: ENST00000409868
  gene symbol: DCTN1
  hgvsc: ENST00000409868.1:c.1650+15T>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386843
  ensembl transcript: ENST00000409567
  gene symbol: DCTN1
  hgvsc: ENST00000409567.3:c.1641+15T>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000387270
  ensembl transcript: ENST00000409438
  gene symbol: DCTN1
  hgvsc: ENST00000409438.1:c.1299+15T>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000497666
  gene symbol: DCTN1
  hgvsc: ENST00000497666.1:n.96+217T>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000354791
  ensembl transcript: ENST00000361874
  gene symbol: DCTN1
  hgvsc: ENST00000361874.3:c.1701+15T>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl transcript: ENST00000466110
  gene symbol: DCTN1
  hgvsc: ENST00000466110.1:n.1922+15T>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000416711
  ensembl transcript: ENST00000434055
  gene symbol: DCTN1
  hgvsc: ENST00000434055.1:c.1590+15T>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000377571
  ensembl transcript: ENST00000394003
  gene symbol: DCTN1
  hgvsc: ENST00000394003.3:c.1680+15T>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000386406
  ensembl transcript: ENST00000409240
  gene symbol: DCTN1
  hgvsc: ENST00000409240.1:c.1590+15T>G
  variant of: http://identifiers.org/hgnc/2711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204843
  ensembl protein: ENSP00000384844
  ensembl transcript: ENST00000407639
  gene symbol: DCTN1
  hgvsc: ENST00000407639.2:c.1299+15T>G
  variant of: http://identifiers.org/hgnc/2711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5360
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2520
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3421
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6811
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7030
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3174
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5807
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3704
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4571
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4339
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
reference allele: A

GenotypeQuality
all individuals: 157
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 689
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10321
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1713
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31340
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2718
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1307
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1011
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2810
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 424
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1293
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 587
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3636
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 368
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23804
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2508
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2904
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9830
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1856
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -7.663e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.03e-2

DP
type: SiteQuality
SIO_000300: 7.62601e5

QD
type: SiteQuality
SIO_000300: 8.74e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.368e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
all individuals: 308
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13137
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 956
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1442
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1082
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 569
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1522
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3164
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2255
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29832
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2809
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 131
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 687
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 694
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 585
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9470
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2184
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 344
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2488
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4052
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1580
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.690431519699812e-5
allele num: 21320
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.18e-1

QD
type: SiteQuality
SIO_000300: 2.434e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.5e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.434e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.24e0

DP
type: SiteQuality
SIO_000300: 7.26759e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 6.5e-2

GenotypeDepth
all individuals: 573
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 690
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2160
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1064
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1451
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 571
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13441
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1495
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3159
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29707
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 957
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 584
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 688
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2809
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 113
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.738887309259786e-5
allele num: 21102
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2168
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 342
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4018
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1566
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2470
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9432
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.56e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.099999999999999e-2

QD
type: SiteQuality
SIO_000300: 2.608e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.358e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.099999999999999e-2

DP
type: SiteQuality
SIO_000300: 7.23551e5

GenotypeQuality
all individuals: 2621
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21233
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 869
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2289
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21402
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1159
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2338
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 661
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2805
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 78
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 680
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 579
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 274
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.051071039574004e-5
allele num: 16526
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1030
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1536
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8806
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3380
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1638
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.97e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.348e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.78e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.78e-2

DP
type: SiteQuality
SIO_000300: 6.45163e5

BaseQRankSum
type: SiteQuality
SIO_000300: -8.96e-1

QD
type: SiteQuality
SIO_000300: 1.267e1

GenotypeQuality
all individuals: 331
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 580
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3134
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2098
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 678
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2253
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18970
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 847
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 854
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2804
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1124
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 654
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8678
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3194
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1422
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 266
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1436
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.453278265358803e-5
allele num: 15496
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 928
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.96e-1

FS
type: SiteQuality
SIO_000300: 2.806e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.12e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.19e0

VQSLOD
type: SiteQuality
SIO_000300: 4.1e-2

QD
type: SiteQuality
SIO_000300: 1.163e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 6.26479e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.45e0

GenotypeQuality
all individuals: 199
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1460
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 575
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2710
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 637
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variant carriers: 0

GenotypeQuality
all individuals: 847
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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num of homozygotes: 0

African
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allele count: 1
allele frequency: 3.663003663003663e-4
allele num: 2730
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 12350
num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

ClippingRankSum
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SIO_000300: 6.840000000000001e-1

BaseQRankSum
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InbreedingCoeff
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SIO_000300: -5.04e-2

MQRankSum
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ReadPosRankSum
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MQ
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -7.958e-1

DP
type: SiteQuality
SIO_000300: 5.70227e5

QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 2718
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 512
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 1010
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 12220
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 230
num of homozygotes: 0

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

ClippingRankSum
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SIO_000300: -1.537e0

FS
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SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: 9.88e-1

MQ
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VQSLOD
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QD
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InbreedingCoeff
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MQRankSum
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SIO_000300: -1.537e0

ReadPosRankSum
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SIO_000300: 4.06e-1

DP
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SIO_000300: 5.6778e5

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8150
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 754
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 11270
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 226
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
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MQRankSum
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SIO_000300: 6.840000000000001e-1

BaseQRankSum
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InbreedingCoeff
type: SiteQuality
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DP
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ClippingRankSum
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SIO_000300: 7.27e-1

MQ
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SIO_000300: 6.0e1

QD
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ReadPosRankSum
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SIO_000300: -7.27e-1

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 10782
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.138952164009112e-3
allele num: 878
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 708
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 392
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

QD
type: SiteQuality
SIO_000300: 7.66e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

InbreedingCoeff
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VQSLOD
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 5.56943e5

MQ
type: SiteQuality
SIO_000300: 5.902e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

African
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allele count: 1
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allele num: 10392
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66646
num of homozygotes: 0

East Asian
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Other
type: Population
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allele frequency: 0.0e0
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ClippingRankSum
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VQSLOD
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MQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.975e1

InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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FS
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.554e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
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Other
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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South Asian
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allele num: 16486
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FS
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QD
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InbreedingCoeff
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MQ
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MQRankSum
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 66646
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South Asian
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African
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European (Finnish)
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Other
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East Asian
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Latino
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QD
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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FS
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DP
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BaseQRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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European (Finnish)
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Other
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East Asian
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European (Non-Finnish)
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VQSLOD
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MQ
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InbreedingCoeff
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BaseQRankSum
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FS
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ReadPosRankSum
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ClippingRankSum
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QD
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Other
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Latino
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East Asian
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African
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South Asian
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European (Non-Finnish)
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InbreedingCoeff
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BaseQRankSum
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DP
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ClippingRankSum
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FS
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MQ
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MQRankSum
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QD
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VQSLOD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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Latino
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European (Non-Finnish)
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South Asian
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African
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Other
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VQSLOD
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ReadPosRankSum
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DP
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BaseQRankSum
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QD
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FS
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InbreedingCoeff
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MQ
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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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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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European (Non-Finnish)
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South Asian
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Other
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Latino
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East Asian
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ClippingRankSum
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MQ
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FS
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BaseQRankSum
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DP
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MQRankSum
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QD
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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South Asian
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African
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Latino
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allele num: 11556
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European (Finnish)
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BaseQRankSum
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VQSLOD
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QD
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InbreedingCoeff
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MQ
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ClippingRankSum
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ReadPosRankSum
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FS
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MQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Other
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African
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South Asian
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Latino
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East Asian
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European (Finnish)
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ClippingRankSum
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MQRankSum
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DP
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VQSLOD
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FS
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QD
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InbreedingCoeff
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MQ
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ReadPosRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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African
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Other
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European (Finnish)
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South Asian
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InbreedingCoeff
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ReadPosRankSum
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QD
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MQRankSum
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BaseQRankSum
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FS
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ClippingRankSum
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MQ
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VQSLOD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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European (Non-Finnish)
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African
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East Asian
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Latino
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South Asian
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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FS
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MQ
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MQRankSum
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QD
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BaseQRankSum
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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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Latino
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European (Non-Finnish)
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East Asian
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South Asian
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African
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European (Finnish)
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InbreedingCoeff
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QD
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ClippingRankSum
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MQRankSum
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FS
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MQ
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VQSLOD
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DP
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BaseQRankSum
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.202643171806168e-3
allele num: 908
num of homozygotes: 1

MQRankSum
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SIO_000300: -3.26e-1

FS
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SIO_000300: 5.287e0

ClippingRankSum
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SIO_000300: 1.68e0

VQSLOD
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SIO_000300: -7.77e-1

DP
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SIO_000300: 2.138614e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.38e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.069e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e-1

QD
type: SiteQuality
SIO_000300: 2.429e1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.907e1

ReadPosRankSum
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SIO_000300: 9.5e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
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SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.437e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.466e0

VQSLOD
type: SiteQuality
SIO_000300: 1.51e0

MQRankSum
type: SiteQuality
SIO_000300: 6.4e-2

DP
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SIO_000300: 2.139154e6

QD
type: SiteQuality
SIO_000300: 1.24e1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

East Asian
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allele count: 2
allele frequency: 2.31107002542177e-4
allele num: 8654
num of homozygotes: 0

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

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

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -5.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.97e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

MQRankSum
type: SiteQuality
SIO_000300: -3.65e-1

InbreedingCoeff
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SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.989e0

VQSLOD
type: SiteQuality
SIO_000300: 1.84e0

QD
type: SiteQuality
SIO_000300: 1.418e1

DP
type: SiteQuality
SIO_000300: 2.139233e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

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

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

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

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

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

DP
type: SiteQuality
SIO_000300: 2.139352e6

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.75e-1

MQ
type: SiteQuality
SIO_000300: 5.98e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.65e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.31e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.889e0

QD
type: SiteQuality
SIO_000300: 1.271e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 3
allele frequency: 2.591568762957844e-4
allele num: 11576
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

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

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

South Asian
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allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.3e-1

BaseQRankSum
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DP
type: SiteQuality
SIO_000300: 2.139523e6

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.634e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 9.64e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

QD
type: SiteQuality
SIO_000300: 1.092e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

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

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

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -9.330000000000001e-1

QD
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MQ
type: SiteQuality
SIO_000300: 5.956e1

FS
type: SiteQuality
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InbreedingCoeff
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MQRankSum
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VQSLOD
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DP
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ClippingRankSum
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SIO_000300: -3.75e-1

ReadPosRankSum
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.13943e6

MQRankSum
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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QD
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FS
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

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

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

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

East Asian
type: Population
allele count: 12
allele frequency: 1.386642015253062e-3
allele num: 8654
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.96e1

VQSLOD
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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DP
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SIO_000300: 2.140203e6

FS
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InbreedingCoeff
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SIO_000300: -1.0e-4

QD
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MQRankSum
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SIO_000300: 6.0e-3

GenotypeQuality
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variant carriers: 0

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

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

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

South Asian
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allele num: 16512
num of homozygotes: 0

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

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

European (Finnish)
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num of homozygotes: 0

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

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

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num of homozygotes: 0

African
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Other
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66740
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East Asian
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South Asian
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ReadPosRankSum
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DP
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ClippingRankSum
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QD
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MQ
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VQSLOD
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FS
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Other
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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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South Asian
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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ReadPosRankSum
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FS
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QD
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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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GenotypeQuality
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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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European (Non-Finnish)
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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FS
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VQSLOD
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QD
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DP
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MQ
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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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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

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

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

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

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

VQSLOD
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ClippingRankSum
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QD
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MQ
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InbreedingCoeff
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DP
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SIO_000300: 2.139588e6

MQRankSum
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FS
type: SiteQuality
SIO_000300: 1.004e0

BaseQRankSum
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SIO_000300: -2.191e0

ReadPosRankSum
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SIO_000300: 1.78e0

GenotypeQuality
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variant carriers: 0

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

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

Latino
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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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num of homozygotes: 0

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

African
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allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
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allele frequency: 1.101321585903084e-3
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ClippingRankSum
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SIO_000300: -1.067e0

QD
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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FS
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MQ
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DP
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SIO_000300: 2.139594e6

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

East Asian
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allele frequency: 2.311604253351826e-4
allele num: 8652
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

BaseQRankSum
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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QD
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FS
type: SiteQuality
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ClippingRankSum
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DP
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SIO_000300: 2.139517e6

MQRankSum
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SIO_000300: 4.0e-3

MQ
type: SiteQuality
SIO_000300: 5.978e1

GenotypeQuality
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variant carriers: 0

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

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

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

Other
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allele count: 0
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num of homozygotes: 0

African
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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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num of homozygotes: 0

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

South Asian
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VQSLOD
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SIO_000300: 1.08e0

ReadPosRankSum
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DP
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MQ
type: SiteQuality
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BaseQRankSum
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SIO_000300: -6.2e-2

ClippingRankSum
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

FS
type: SiteQuality
SIO_000300: 3.423e0

QD
type: SiteQuality
SIO_000300: 1.32e1

GenotypeQuality
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variant carriers: 0

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

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

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

Other
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allele 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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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.49902563333833e-5
allele num: 66710
num of homozygotes: 0

Latino
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FS
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VQSLOD
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MQ
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ReadPosRankSum
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DP
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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QD
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InbreedingCoeff
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GenotypeDepth
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variant carriers: 1

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

South Asian
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allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

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

European (Finnish)
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num of homozygotes: 0

European (Non-Finnish)
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East Asian
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African
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Other
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Latino
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South Asian
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VQSLOD
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InbreedingCoeff
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FS
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MQ
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ReadPosRankSum
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DP
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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East Asian
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European (Finnish)
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South Asian
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European (Non-Finnish)
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Other
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MQ
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MQRankSum
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BaseQRankSum
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DP
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VQSLOD
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InbreedingCoeff
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FS
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ReadPosRankSum
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ClippingRankSum
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QD
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GenotypeQuality
all individuals: 50
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 8702
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variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66676
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.653513326410523e-5
allele num: 11556
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -9.006e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

QD
type: SiteQuality
SIO_000300: 1.811e1

DP
type: SiteQuality
SIO_000300: 2.134183e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.49e0

FS
type: SiteQuality
SIO_000300: 4.306e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.11e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.9e0

MQ
type: SiteQuality
SIO_000300: 5.943e1

GenotypeQuality
all individuals: 8622
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66652
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.313208420078649e-4
allele num: 8646
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.9e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.5e-1

FS
type: SiteQuality
SIO_000300: 5.281e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 1.116e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.593e0

DP
type: SiteQuality
SIO_000300: 2.128325e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e-1

GenotypeQuality
all individuals: 80
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1947
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 16

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 184
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variant carriers: 0

GenotypeQuality
all individuals: 22392
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66636
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 16
allele frequency: 9.700497150478962e-4
allele num: 16494
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.963e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.672e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.84e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.2e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.15e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.84e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.1272e6

QD
type: SiteQuality
SIO_000300: 1.256e1

GenotypeQuality
all individuals: 362
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 262
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variant carriers: 0

GenotypeQuality
all individuals: 4206
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66604
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.632055480639569e-5
allele num: 10382
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.158480074142725e-4
allele num: 8632
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.581e0

VQSLOD
type: SiteQuality
SIO_000300: 2.6e-3

QD
type: SiteQuality
SIO_000300: 8.33e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.34e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.84e0

FS
type: SiteQuality
SIO_000300: 2.233e0

MQRankSum
type: SiteQuality
SIO_000300: 3.34e-1

DP
type: SiteQuality
SIO_000300: 2.122271e6

MQ
type: SiteQuality
SIO_000300: 5.97e1

GenotypeQuality
all individuals: 336
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 351
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66590
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.477857639693948e-4
allele num: 8626
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.562e0

MQRankSum
type: SiteQuality
SIO_000300: 7.55e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 6.07e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

QD
type: SiteQuality
SIO_000300: 1.082e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.9e-1

DP
type: SiteQuality
SIO_000300: 2.117869e6

VQSLOD
type: SiteQuality
SIO_000300: 6.54e-1

GenotypeQuality
all individuals: 390
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 174
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10374
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.671522719389525e-5
allele num: 11532
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66582
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.59e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.09e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.55e-1

FS
type: SiteQuality
SIO_000300: 8.321e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.9e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.48e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.867e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.114059e6

GenotypeQuality
all individuals: 139
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 4.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.510439510920179e-5
allele num: 66574
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.439e0

DP
type: SiteQuality
SIO_000300: 2.110339e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

MQRankSum
type: SiteQuality
SIO_000300: 1.42e-1

FS
type: SiteQuality
SIO_000300: 4.573e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.58e-1

MQ
type: SiteQuality
SIO_000300: 5.948e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

QD
type: SiteQuality
SIO_000300: 2.415e1

GenotypeQuality
all individuals: 854
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 8343
bin: 6.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66544
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16480
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.734304543877905e-4
allele num: 11532
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.106774e6

QD
type: SiteQuality
SIO_000300: 1.439e1

InbreedingCoeff
type: SiteQuality
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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FS
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MQ
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BaseQRankSum
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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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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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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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East Asian
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Other
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MQRankSum
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InbreedingCoeff
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VQSLOD
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MQ
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QD
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DP
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FS
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ClippingRankSum
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Other
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African
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European (Non-Finnish)
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Latino
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East Asian
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allele num: 8604
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European (Finnish)
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allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
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MQ
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MQRankSum
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DP
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ClippingRankSum
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FS
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BaseQRankSum
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QD
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ReadPosRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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Other
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Latino
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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VQSLOD
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ReadPosRankSum
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DP
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ClippingRankSum
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MQRankSum
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MQ
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FS
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QD
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InbreedingCoeff
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Other
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele num: 11504
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East Asian
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African
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South Asian
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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FS
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InbreedingCoeff
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MQ
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ClippingRankSum
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QD
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VQSLOD
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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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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

Latino
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European (Finnish)
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Other
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South Asian
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European (Non-Finnish)
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allele num: 66324
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African
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FS
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ClippingRankSum
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QD
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MQRankSum
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DP
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MQ
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Other
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African
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European (Finnish)
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Latino
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East Asian
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South Asian
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VQSLOD
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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DP
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MQ
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QD
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FS
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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Latino
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African
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Other
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European (Non-Finnish)
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South Asian
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MQRankSum
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DP
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BaseQRankSum
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FS
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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MQ
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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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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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European (Finnish)
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Latino
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African
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Other
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European (Non-Finnish)
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FS
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DP
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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SIO_000300: 4.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.65e-1

MQ
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SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.55e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.76e0

QD
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SIO_000300: 1.292e1

GenotypeQuality
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variant carriers: 0

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

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

Latino
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allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

BaseQRankSum
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SIO_000300: 3.28e0

MQ
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SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: -1.0e-4

QD
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ReadPosRankSum
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DP
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VQSLOD
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FS
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ClippingRankSum
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SIO_000300: -2.47e0

MQRankSum
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SIO_000300: -1.335e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 11574
num of homozygotes: 0

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

East Asian
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allele frequency: 2.31107002542177e-4
allele num: 8654
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

ReadPosRankSum
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SIO_000300: -1.57e-1

FS
type: SiteQuality
SIO_000300: 2.102e0

VQSLOD
type: SiteQuality
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QD
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MQ
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ClippingRankSum
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BaseQRankSum
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SIO_000300: -1.836e0

InbreedingCoeff
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SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 3.337724e6

MQRankSum
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SIO_000300: 3.18e-1

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

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

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.909e0

MQRankSum
type: SiteQuality
SIO_000300: 9.89e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.07e0

InbreedingCoeff
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SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 7.11e-1

ReadPosRankSum
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SIO_000300: 3.61e-1

DP
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SIO_000300: 3.338339e6

BaseQRankSum
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SIO_000300: -2.212e0

QD
type: SiteQuality
SIO_000300: 1.204e1

MQ
type: SiteQuality
SIO_000300: 5.927e1

GenotypeQuality
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variant carriers: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.988e1

MQRankSum
type: SiteQuality
SIO_000300: -1.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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QD
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VQSLOD
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FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 3.339034e6

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

Other
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num of homozygotes: 0

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

Latino
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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FS
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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MQ
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MQRankSum
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DP
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QD
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GenotypeQuality
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variant carriers: 0

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

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

Other
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num of homozygotes: 0

African
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East 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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allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

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

African
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allele num: 10394
num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

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

East Asian
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num of homozygotes: 0

European (Finnish)
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Other
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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 num: 66738
num of homozygotes: 0

Latino
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num of homozygotes: 0

South Asian
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ClippingRankSum
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MQ
type: SiteQuality
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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FS
type: SiteQuality
SIO_000300: 4.994e0

QD
type: SiteQuality
SIO_000300: 8.960000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.512e0

VQSLOD
type: SiteQuality
SIO_000300: 1.9e-2

DP
type: SiteQuality
SIO_000300: 3.339626e6