14-75355750-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355750
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355750
    reference: chr 14
allele count: 1
allele frequency: 8.305509875251242e-6
allele num: 120402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.-3-228G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.147-48G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.50-48G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.96-48G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.151-48G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.179-48G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.147-48G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.147-48G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.113-228G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.187-48G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.113-48G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.142-228G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.93-48G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.98-48G>T
  variant of: http://identifiers.org/hgnc/2911
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4753
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5923
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3225
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7659
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5064
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3617
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6509
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8380
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP

14-75355757-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355757
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355757
    reference: chr 14
allele count: 1
allele frequency: 9.564252649297984e-6
allele num: 104556
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.50-41G>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.147-41G>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.142-221G>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.93-41G>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.147-41G>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.-3-221G>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.113-41G>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.98-41G>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.113-221G>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.187-41G>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.147-41G>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.179-41G>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.96-41G>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.151-41G>C
  variant of: http://identifiers.org/hgnc/2911
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7974
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2855
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5192
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8651
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: African
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff

14-75355760-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355760
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355760
    reference: chr 14
allele count: 1
allele frequency: 1.121931517300184e-5
allele num: 89132
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.151-38C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.98-38C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.147-38C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.142-218C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.147-38C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.179-38C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.93-38C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.187-38C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.96-38C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.50-38C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.113-218C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.113-38C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.-3-218C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.147-38C>T
  variant of: http://identifiers.org/hgnc/2911
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1729
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2507
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3881
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6561
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4407
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7978
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD

14-75355763-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355763
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355763
    reference: chr 14
allele count: 23
allele frequency: 2.963688374610211e-4
allele num: 77606
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.151-35C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.142-215C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.-3-215C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.147-35C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.50-35C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.147-35C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.113-215C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.93-35C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.113-35C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.147-35C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.98-35C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.187-35C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.179-35C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.96-35C>T
  variant of: http://identifiers.org/hgnc/2911
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3669
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3165
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4916
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6149
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2619
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5030
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD

14-75355767-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355767
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355766
    reference: chr 14
allele count: 71328
allele frequency: 5.878939733614664e-1
allele num: 121328
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.50-27delA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.96-27delA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.147-27delA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.113-27delA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.179-27delA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.187-27delA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.113-207delA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.98-27delA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.93-27delA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.147-27delA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.142-207delA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.147-27delA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.151-27delA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.-3-207delA
  variant of: http://identifiers.org/hgnc/2911
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4315
  bin: 7.25e1
  variant carriers: 4096
genotype depth: GenotypeDepth
  all individuals: 5826
  bin: 5.75e1
  variant carriers: 4902
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 2.75e1
  variant carriers: 423
genotype depth: GenotypeDepth
  all individuals: 3149
  bin: 3.75e1
  variant carriers: 1748
genotype depth: GenotypeDepth
  all individuals: 5635
  bin: 5.25e1
  variant carriers: 4328
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 2063
  bin: 3.25e1
  variant carriers: 977
genotype depth: GenotypeDepth
  all individuals: 5732
  bin: 6.25e1
  variant carriers: 5132
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 5108
  bin: 4.75e1
  variant carriers: 3557
genotype depth: GenotypeDepth
  all individuals: 3584
  bin: 7.75e1
  variant carriers: 3419
genotype depth: GenotypeDepth
  all individuals: 1933
  bin: 8.75e1
  variant carriers: 1851
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 21922
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
reference allele: TA
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/14-75355769-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355769
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355769
    reference: chr 14
allele count: 1
allele frequency: 4.440103010389841e-5
allele num: 22522
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.113-29A>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.147-29A>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.151-29A>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.147-29A>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.147-29A>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.-3-209A>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.187-29A>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.179-29A>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.113-209A>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.93-29A>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.50-29A>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.98-29A>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.142-209A>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.96-29A>C
  variant of: http://identifiers.org/hgnc/2911
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4691
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2757
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2725
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1798
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2539
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2703
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: FS

http://identifiers.org/exac.variant/14-75355770-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355770
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355770
    reference: chr 14
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.151-28A>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.187-28A>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.113-28A>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.113-208A>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.179-28A>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.147-28A>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.-3-208A>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.96-28A>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.147-28A>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.50-28A>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.93-28A>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.98-28A>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.147-28A>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.142-208A>C
  variant of: http://identifiers.org/hgnc/2911
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6514
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4368
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6286
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1667
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3451
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4744
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3182
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5716
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1731
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ

14-75355771-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355771
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355771
    reference: chr 14
allele count: 2
allele frequency: 1.648723063986942e-5
allele num: 121306
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.113-27A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.96-27A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.147-27A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.147-27A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.-3-207A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.113-207A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.98-27A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.147-27A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.142-207A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.179-27A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.187-27A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.151-27A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.50-27A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.93-27A>G
  variant of: http://identifiers.org/hgnc/2911
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4368
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3450
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4744
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1665
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3184
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1731
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5715
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5528
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5750
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6515
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

14-75355781-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355781
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355781
    reference: chr 14
allele count: 25
allele frequency: 2.059443785422433e-4
allele num: 121392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.96-17G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.113-197G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.113-17G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.-3-197G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.147-17G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.151-17G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.147-17G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.93-17G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.10G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.147-17G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.50-17G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.142-197G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.98-17G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.187-17G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.179-17G>A
  variant of: http://identifiers.org/hgnc/2911
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3197
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5525
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5717
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4368
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6289
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3452
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1734
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum

14-75355781-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355781
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355781
    reference: chr 14
allele count: 2
allele frequency: 1.647555028337947e-5
allele num: 121392
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.-3-197G>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.113-197G>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.147-17G>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.147-17G>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.93-17G>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.98-17G>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.179-17G>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.147-17G>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.113-17G>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.10G>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.96-17G>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.187-17G>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.142-197G>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.50-17G>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.151-17G>C
  variant of: http://identifiers.org/hgnc/2911
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3452
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5717
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6289
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5746
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6727
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3197
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

14-75355799-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355799
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355799
    reference: chr 14
allele count: 29
allele frequency: 2.38883671889158e-4
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.97A>T
  hgvsp: ENSP00000451957.1:p.Ile33Phe
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.148A>T
  hgvsp: ENSP00000335304.4:p.Ile50Phe
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.94A>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.113-179A>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.114A>T
  hgvsp: ENST00000555492.1:c.114A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.148A>T
  hgvsp: ENSP00000238671.7:p.Ile50Phe
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.188A>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.28A>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.148A>T
  hgvsp: ENSP00000451210.1:p.Ile50Phe
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.51A>T
  hgvsp: ENSP00000451425.1:p.Ile18Phe
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.180A>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.142-179A>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.-3-179A>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.152A>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.99A>T
  hgvsp: ENST00000555089.1:c.99A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2911
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4368
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6287
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5742
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile50Phe
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

14-75355810-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355810
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355810
    reference: chr 14
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.62T>C
  hgvsp: ENST00000555988.1:c.62T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.105T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.142-168T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.199T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.159T>C
  hgvsp: ENST00000556460.1:c.159T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.108T>C
  hgvsp: ENST00000554806.1:c.108T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.110T>C
  hgvsp: ENSP00000452422.1:p.Val37Ala
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.125T>C
  hgvsp: ENSP00000452417.1:p.Val42Ala
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.159T>C
  hgvsp: ENST00000334220.4:c.159T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.39T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.191T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.159T>C
  hgvsp: ENST00000238671.7:c.159T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.163T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.113-168T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.-3-168T>C
  variant of: http://identifiers.org/hgnc/2911
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5746
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6731
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1735
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6515
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5526
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val37Ala
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

14-75355819-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355819
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355819
    reference: chr 14
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.168T>C
  hgvsp: ENST00000238671.7:c.168T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.71T>C
  hgvsp: ENST00000555988.1:c.71T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.134T>C
  hgvsp: ENSP00000452417.1:p.Val45Ala
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.172T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.168T>C
  hgvsp: ENST00000556460.1:c.168T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.119T>C
  hgvsp: ENSP00000452422.1:p.Val40Ala
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.117T>C
  hgvsp: ENST00000554806.1:c.117T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.113-159T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.208T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.48T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.200T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.114T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.168T>C
  hgvsp: ENST00000334220.4:c.168T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.-3-159T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.142-159T>C
  variant of: http://identifiers.org/hgnc/2911
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1711
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6731
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2495
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1735
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6515
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5716
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6288
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val40Ala
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ

14-75355824-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355824
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355824
    reference: chr 14
allele count: 2
allele frequency: 1.647446457990115e-5
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.122G>A
  hgvsp: ENSP00000451957.1:p.Arg41His
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.177G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.139G>A
  hgvsp: ENSP00000452417.1:p.Ala47Thr
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.205G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.173G>A
  hgvsp: ENSP00000335304.4:p.Arg58His
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.173G>A
  hgvsp: ENSP00000238671.7:p.Arg58His
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.173G>A
  hgvsp: ENSP00000451210.1:p.Arg58His
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.124G>A
  hgvsp: ENSP00000452422.1:p.Ala42Thr
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.119G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.213G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.-3-154G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.53G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.76G>A
  hgvsp: ENSP00000451425.1:p.Arg26His
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.142-154G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.113-154G>A
  variant of: http://identifiers.org/hgnc/2911
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5746
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6288
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4747
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2495
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3191
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4368
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg58His
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

14-75355829-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355829
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355829
    reference: chr 14
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.178T>G
  hgvsp: ENSP00000335304.4:p.Phe60Val
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.58T>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.127T>G
  hgvsp: ENSP00000451957.1:p.Phe43Val
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.144T>G
  hgvsp: ENSP00000452417.1:p.Phe48Leu
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.81T>G
  hgvsp: ENSP00000451425.1:p.Phe28Val
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.182T>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.178T>G
  hgvsp: ENSP00000451210.1:p.Phe60Val
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.129T>G
  hgvsp: ENSP00000452422.1:p.Phe43Leu
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.210T>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.124T>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.178T>G
  hgvsp: ENSP00000238671.7:p.Phe60Val
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.-3-149T>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.142-149T>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.113-149T>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.218T>G
  variant of: http://identifiers.org/hgnc/2911
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3189
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3448
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5526
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1735
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6730
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe60Val
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

14-75355830-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355830
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355830
    reference: chr 14
allele count: 2
allele frequency: 1.647500741375333e-5
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.128T>C
  hgvsp: ENSP00000451957.1:p.Phe43Ser
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.130T>C
  hgvsp: ENSP00000452422.1:p.Ser44Pro
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.179T>C
  hgvsp: ENSP00000451210.1:p.Phe60Ser
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.211T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.142-148T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.179T>C
  hgvsp: ENSP00000335304.4:p.Phe60Ser
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.145T>C
  hgvsp: ENSP00000452417.1:p.Ser49Pro
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.59T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.219T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.82T>C
  hgvsp: ENSP00000451425.1:p.Phe28Ser
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.-3-148T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.113-148T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.183T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.179T>C
  hgvsp: ENSP00000238671.7:p.Phe60Ser
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.125T>C
  variant of: http://identifiers.org/hgnc/2911
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6515
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5746
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe60Ser
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

14-75355831-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355831
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355831
    reference: chr 14
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.-3-147C>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.131C>G
  hgvsp: ENSP00000452422.1:p.Ser44Ter
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.220C>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.180C>G
  hgvsp: ENSP00000238671.7:p.Phe60Leu
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.113-147C>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.83C>G
  hgvsp: ENSP00000451425.1:p.Phe28Leu
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.180C>G
  hgvsp: ENSP00000335304.4:p.Phe60Leu
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.60C>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.180C>G
  hgvsp: ENSP00000451210.1:p.Phe60Leu
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.129C>G
  hgvsp: ENSP00000451957.1:p.Phe43Leu
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.146C>G
  hgvsp: ENSP00000452417.1:p.Ser49Ter
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.184C>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.212C>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.126C>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.142-147C>G
  variant of: http://identifiers.org/hgnc/2911
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5746
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6729
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5527
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4747
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4368
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6515
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser44Ter
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: African
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/14-75355835-AC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355835
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355834
    reference: chr 14
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.189delC
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.151delC
  hgvsp: ENSP00000452417.1:p.Leu51TyrfsTer7
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.185delC
  hgvsp: ENSP00000335304.4:p.Thr62IlefsTer61
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.217delC
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.-3-142delC
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.65delC
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.136delC
  hgvsp: ENSP00000452422.1:p.Leu46TyrfsTer?
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.134delC
  hgvsp: ENSP00000451957.1:p.Thr45IlefsTer61
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.185delC
  hgvsp: ENSP00000451210.1:p.Thr62IlefsTer?
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.88delC
  hgvsp: ENSP00000451425.1:p.Thr30IlefsTer156
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.225delC
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.131delC
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.142-142delC
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.185delC
  hgvsp: ENSP00000238671.7:p.Thr62IlefsTer43
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.113-142delC
  variant of: http://identifiers.org/hgnc/2911
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5746
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1735
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4368
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr62IlefsTer61
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: AC
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

14-75355839-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355839
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355839
    reference: chr 14
allele count: 2
allele frequency: 1.647473599235572e-5
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.188C>T
  hgvsp: ENSP00000238671.7:p.Thr63Ile
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.154C>T
  hgvsp: ENSP00000452417.1:p.Gln52Ter
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.188C>T
  hgvsp: ENSP00000451210.1:p.Thr63Ile
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.113-139C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.220C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.139C>T
  hgvsp: ENSP00000452422.1:p.Gln47Ter
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.91C>T
  hgvsp: ENSP00000451425.1:p.Thr31Ile
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.137C>T
  hgvsp: ENSP00000451957.1:p.Thr46Ile
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.192C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.-3-139C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.68C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.188C>T
  hgvsp: ENSP00000335304.4:p.Thr63Ile
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.134C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.142-139C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.228C>T
  variant of: http://identifiers.org/hgnc/2911
canonical: false
consequence: stop gained
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 1735
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5745
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6516
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4368
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3448
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln47Ter
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum

14-75355840-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355840
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355840
    reference: chr 14
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.113-138A>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.-3-138A>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.155A>T
  hgvsp: ENSP00000452417.1:p.Gln52Leu
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.189A>T
  hgvsp: ENST00000238671.7:c.189A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.193A>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.221A>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.138A>T
  hgvsp: ENST00000554806.1:c.138A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.135A>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.69A>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.189A>T
  hgvsp: ENST00000334220.4:c.189A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.92A>T
  hgvsp: ENST00000555988.1:c.92A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.140A>T
  hgvsp: ENSP00000452422.1:p.Gln47Leu
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.189A>T
  hgvsp: ENST00000556460.1:c.189A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.229A>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.142-138A>T
  variant of: http://identifiers.org/hgnc/2911
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4368
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3448
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln47Leu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum

14-75355844-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355844
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355844
    reference: chr 14
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.159G>A
  hgvsp: ENST00000555492.1:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.142-134G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.142G>A
  hgvsp: ENSP00000451957.1:p.Val48Ile
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.113-134G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.139G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.-3-134G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.193G>A
  hgvsp: ENSP00000335304.4:p.Val65Ile
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.96G>A
  hgvsp: ENSP00000451425.1:p.Val33Ile
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.144G>A
  hgvsp: ENST00000555089.1:c.144G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.225G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.193G>A
  hgvsp: ENSP00000238671.7:p.Val65Ile
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.193G>A
  hgvsp: ENSP00000451210.1:p.Val65Ile
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.197G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.73G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.233G>A
  variant of: http://identifiers.org/hgnc/2911
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4747
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3448
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5717
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val65Ile
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/14-75355858-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355858
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355858
    reference: chr 14
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.79+8C>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.113-120C>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.231+8C>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.239+8C>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.199+8C>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.203+8C>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.199+8C>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.142-120C>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.148+8C>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.199+8C>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.145+8C>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.-3-120C>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.165+8C>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.102+8C>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.150+8C>A
  variant of: http://identifiers.org/hgnc/2911
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5526
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3188
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6516
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4747
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1734
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.199+8C>A
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
reference allele: C
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

14-75355870-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355870
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355870
    reference: chr 14
allele count: 3
allele frequency: 2.471251112063001e-5
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.199+20G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.79+20G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.148+20G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.165+20G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.142-108G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.199+20G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.150+20G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.102+20G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.-3-108G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.145+20G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.231+20G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.199+20G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.113-108G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.203+20G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.239+20G>A
  variant of: http://identifiers.org/hgnc/2911
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4366
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1735
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3185
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5527
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5716
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff

14-75355884-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355884
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355884
    reference: chr 14
allele count: 7
allele frequency: 5.766252594813668e-5
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.148+34T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.113-94T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.145+34T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.102+34T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.199+34T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.165+34T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.79+34T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.-3-94T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.150+34T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.203+34T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.199+34T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.239+34T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.199+34T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.142-94T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.231+34T>C
  variant of: http://identifiers.org/hgnc/2911
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6291
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5746
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6730
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4746
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5524
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3448
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3163
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4357
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: African
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

http://identifiers.org/exac.variant/14-75355896-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355896
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355896
    reference: chr 14
allele count: 2
allele frequency: 1.647907980818351e-5
allele num: 121366
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.165+46C>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.79+46C>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.148+46C>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.142-82C>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.145+46C>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.199+46C>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.150+46C>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.203+46C>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.113-82C>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.-3-82C>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.199+46C>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.102+46C>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.231+46C>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.239+46C>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.199+46C>A
  variant of: http://identifiers.org/hgnc/2911
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2497
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4746
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6729
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3036
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: QD
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

14-75355896-CAATT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355896
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355892
    reference: chr 14
allele count: 3
allele frequency: 2.471861971227527e-5
allele num: 121366
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.231+47_231+50delAATT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.203+47_203+50delAATT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.142-81_142-78delAATT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.145+47_145+50delAATT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.150+47_150+50delAATT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.102+47_102+50delAATT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.-3-81_-3-78delAATT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.113-81_113-78delAATT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.239+47_239+50delAATT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.199+47_199+50delAATT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.199+47_199+50delAATT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.199+47_199+50delAATT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.79+47_79+50delAATT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.165+47_165+50delAATT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.148+47_148+50delAATT
  variant of: http://identifiers.org/hgnc/2911
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4746
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4331
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3036
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6515
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6287
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: CAATT
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ

14-75355898-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355898
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355898
    reference: chr 14
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.165+48A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.239+48A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.102+48A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.142-80A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.203+48A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.79+48A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.150+48A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.148+48A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.199+48A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.199+48A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.199+48A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.231+48A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.-3-80A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.145+48A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.113-80A>G
  variant of: http://identifiers.org/hgnc/2911
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2989
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6730
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6515
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6286
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3449
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5715
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5501
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

14-75355898-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355898
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355897
    reference: chr 14
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.79+50delT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.145+50delT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.-3-78delT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.113-78delT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.239+50delT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.102+50delT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.165+50delT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.199+50delT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.150+50delT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.148+50delT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.199+50delT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.199+50delT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.142-78delT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.231+50delT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.203+50delT
  variant of: http://identifiers.org/hgnc/2911
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6730
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3449
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5743
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6515
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6286
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4312
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2497
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: AT
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

14-75355900-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355900
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355900
    reference: chr 14
allele count: 144
allele frequency: 1.187178472497032e-3
allele num: 121296
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.79+50T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.102+50T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.199+50T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.239+50T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.231+50T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.145+50T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.165+50T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.150+50T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.-3-78T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.113-78T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.148+50T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.199+50T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.142-78T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.203+50T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.199+50T>C
  variant of: http://identifiers.org/hgnc/2911
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2930
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4240
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 5475
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2498
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 5740
  bin: 6.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1686
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1732
  bin: 8.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

14-75355927-TAAA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355927
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355924
    reference: chr 14
allele count: 14
allele frequency: 1.165442951567521e-4
allele num: 120126
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.166-48_166-46delAAA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.80-48_80-46delAAA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.240-48_240-46delAAA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.142-48_142-46delAAA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.200-50_200-48delAAA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.-3-48_-3-46delAAA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.113-48_113-46delAAA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.151-50_151-48delAAA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.232-48_232-46delAAA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.149-48_149-46delAAA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.200-48_200-46delAAA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.103-48_103-46delAAA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.146-48_146-46delAAA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.200-48_200-46delAAA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.204-48_204-46delAAA
  variant of: http://identifiers.org/hgnc/2911
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3040
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2770
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4124
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7385
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8514
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: TAAA
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

14-75355928-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355928
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355928
    reference: chr 14
allele count: 1
allele frequency: 8.330834083108401e-6
allele num: 120036
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.240-50A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.142-50A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.149-50A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.166-50A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.113-50A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.200-50A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.80-50A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.151-52A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.103-50A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.200-52A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.232-50A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.-3-50A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.200-50A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.146-50A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.204-50A>G
  variant of: http://identifiers.org/hgnc/2911
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12301
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8509
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4121
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3210
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1815
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12896
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

14-75355931-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355931
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355931
    reference: chr 14
allele count: 19
allele frequency: 1.581540920290338e-4
allele num: 120136
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.200-47A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.240-47A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.80-47A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.103-47A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.200-47A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.142-47A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.149-47A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.200-49A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.-3-47A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.151-49A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.204-47A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.166-47A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.146-47A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.113-47A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.232-47A>G
  variant of: http://identifiers.org/hgnc/2911
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1818
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7267
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2750
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3269
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8505
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

14-75355951-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355951
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355951
    reference: chr 14
allele count: 4
allele frequency: 3.326292680492956e-5
allele num: 120254
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.113-27T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.-3-27T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.166-27T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.200-29T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.204-27T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.200-27T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.103-27T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.240-27T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.149-27T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.146-27T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.200-27T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.80-27T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.151-29T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.142-27T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.232-27T>C
  variant of: http://identifiers.org/hgnc/2911
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8494
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4115
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12913
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4905
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1331
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: T
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

14-75355952-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355952
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355952
    reference: chr 14
allele count: 1
allele frequency: 8.317253310266817e-6
allele num: 120232
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.151-28G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.200-26G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.200-28G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.232-26G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.142-26G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.-3-26G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.113-26G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.80-26G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.166-26G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.149-26G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.204-26G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.200-26G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.240-26G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.103-26G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.146-26G>A
  variant of: http://identifiers.org/hgnc/2911
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12341
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4117
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7424
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12914
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

14-75355953-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355953
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355954
    reference: chr 14
allele count: 6
allele frequency: 4.988526389304599e-5
allele num: 120276
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.113-21dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.149-21dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.200-21dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.-3-21dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.146-21dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.240-21dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.80-21dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.204-21dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.151-23dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.103-21dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.166-21dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.232-21dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.142-21dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.200-21dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.200-23dupT
  variant of: http://identifiers.org/hgnc/2911
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8493
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12920
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4115
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7453
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5110
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum

14-75355958-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355958
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355958
    reference: chr 14
allele count: 1
allele frequency: 8.313242996092776e-6
allele num: 120290
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.166-20C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.151-22C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.200-20C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.113-20C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.240-20C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.80-20C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.232-20C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.-3-20C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.200-22C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.204-20C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.142-20C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.103-20C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.200-20C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.149-20C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.146-20C>T
  variant of: http://identifiers.org/hgnc/2911
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8495
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7527
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4116
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5486
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12928
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

14-75355965-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355965
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355965
    reference: chr 14
allele count: 1
allele frequency: 8.301648707433296e-6
allele num: 120458
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.232-13G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.166-13G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.200-15G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.103-13G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.151-15G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.113-13G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.146-13G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.200-13G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.80-13G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.240-13G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.149-13G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.200-13G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.142-13G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.-3-13G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.204-13G>T
  variant of: http://identifiers.org/hgnc/2911
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7674
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12404
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4113
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6036
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8490
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

14-75355978-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355978
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355978
    reference: chr 14
allele count: 3
allele frequency: 2.483978339708878e-5
allele num: 120774
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.204A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.240A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.151-2A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.-3A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.142A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.149A>G
  hgvsp: ENSP00000451957.1:p.Lys50Arg
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.103A>G
  hgvsp: ENSP00000451425.1:p.Lys35Arg
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.232A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: stop_lost
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.113A>G
  hgvsp: ENSP00000451670.1:p.Ter38TrpextTer38
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.200A>G
  hgvsp: ENSP00000451210.1:p.Lys67Arg
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.80A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.146A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.200A>G
  hgvsp: ENSP00000335304.4:p.Lys67Arg
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.200-2A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.166A>G
  hgvsp: ENSP00000452417.1:p.Arg56Gly
  variant of: http://identifiers.org/hgnc/2911
canonical: false
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4112
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8485
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6772
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.151-2A>G
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

14-75355978-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355978
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355978
    reference: chr 14
allele count: 1
allele frequency: 8.279927799029592e-6
allele num: 120774
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_lost
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.113A>T
  hgvsp: ENSP00000451670.1:p.Ter38LeuextTer38
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.151-2A>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.200-2A>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.149A>T
  hgvsp: ENSP00000451957.1:p.Lys50Met
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.204A>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.232A>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.240A>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.166A>T
  hgvsp: ENSP00000452417.1:p.Arg56Trp
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.200A>T
  hgvsp: ENSP00000335304.4:p.Lys67Met
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.103A>T
  hgvsp: ENSP00000451425.1:p.Lys35Met
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.-3A>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.200A>T
  hgvsp: ENSP00000451210.1:p.Lys67Met
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.80A>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.146A>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.142A>T
  variant of: http://identifiers.org/hgnc/2911
canonical: false
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6772
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12462
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7904
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.151-2A>T
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: Other
reference allele: A
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff

14-75355981-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355981
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355981
    reference: chr 14
allele count: 4
allele frequency: 3.310984190050492e-5
allele num: 120810
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.*2A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.169A>G
  hgvsp: ENSP00000452417.1:p.Met57Val
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.152A>G
  hgvsp: ENSP00000452422.1:p.Asp51Gly
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.83A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.152A>G
  hgvsp: ENSP00000451957.1:p.Asp51Gly
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.235A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.203A>G
  hgvsp: ENSP00000451210.1:p.Asp68Gly
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.201A>G
  hgvsp: ENST00000238671.7:c.201A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.1A>G
  hgvsp: ENSP00000335465.6:p.Met1?
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.149A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.145A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.207A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.243A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.106A>G
  hgvsp: ENSP00000451425.1:p.Asp36Gly
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.203A>G
  hgvsp: ENSP00000335304.4:p.Asp68Gly
  variant of: http://identifiers.org/hgnc/2911
canonical: false
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12467
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12943
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4112
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7943
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met1?
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

14-75355992-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75355992
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75355992
    reference: chr 14
allele count: 3
allele frequency: 2.480774001488464e-5
allele num: 120930
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.*8A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.214A>G
  hgvsp: ENSP00000335304.4:p.Thr72Ala
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.117A>G
  hgvsp: ENSP00000451425.1:p.Thr40Ala
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.246A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.214A>G
  hgvsp: ENSP00000451210.1:p.Thr72Ala
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.180A>G
  hgvsp: ENST00000555492.1:c.180A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.218A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.94A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.*13A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.163A>G
  hgvsp: ENSP00000451957.1:p.Thr55Ala
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.163A>G
  hgvsp: ENSP00000452422.1:p.Thr55Ala
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.156A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.12A>G
  hgvsp: ENST00000334212.6:c.12A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.254A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.160A>G
  variant of: http://identifiers.org/hgnc/2911
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12940
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8489
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4111
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12474
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8033
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr72Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

14-75356007-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75356007
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75356007
    reference: chr 14
allele count: 1
allele frequency: 8.269656974628692e-6
allele num: 120924
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.229G>A
  hgvsp: ENSP00000451210.1:p.Ala77Thr
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.269G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.109G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.*23G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.132G>A
  hgvsp: ENSP00000451425.1:p.Ala45Thr
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.178G>A
  hgvsp: ENSP00000452422.1:p.Ala60Thr
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.229G>A
  hgvsp: ENSP00000335304.4:p.Ala77Thr
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.195G>A
  hgvsp: ENST00000555492.1:c.195G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.233G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.178G>A
  hgvsp: ENSP00000451957.1:p.Ala60Thr
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.*28G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.171G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.261G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.27G>A
  hgvsp: ENST00000334212.6:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.175G>A
  variant of: http://identifiers.org/hgnc/2911
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala77Thr
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP

14-75356008-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75356008
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75356008
    reference: chr 14
allele count: 2
allele frequency: 1.653986106516705e-5
allele num: 120920
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.270C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.230C>T
  hgvsp: ENSP00000335304.4:p.Ala77Val
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.196C>T
  hgvsp: ENSP00000452417.1:p.Arg66Cys
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.172C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.28C>T
  hgvsp: ENSP00000335465.6:p.Arg10Cys
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.230C>T
  hgvsp: ENSP00000451210.1:p.Ala77Val
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.*24C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.133C>T
  hgvsp: ENSP00000451425.1:p.Ala45Val
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.262C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.179C>T
  hgvsp: ENSP00000452422.1:p.Ala60Val
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.179C>T
  hgvsp: ENSP00000451957.1:p.Ala60Val
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.*29C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.234C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.176C>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.110C>T
  variant of: http://identifiers.org/hgnc/2911
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6848
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1289
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12946
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala77Val
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

14-75356009-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75356009
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75356009
    reference: chr 14
allele count: 2
allele frequency: 1.654013463669594e-5
allele num: 120918
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.271G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.231G>A
  hgvsp: ENST00000556460.1:c.231G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.180G>A
  hgvsp: ENST00000554806.1:c.180G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.173G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.263G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.235G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.177G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.180G>A
  hgvsp: ENST00000555089.1:c.180G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.29G>A
  hgvsp: ENSP00000335465.6:p.Arg10His
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.197G>A
  hgvsp: ENSP00000452417.1:p.Arg66His
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.134G>A
  hgvsp: ENST00000555988.1:c.134G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.231G>A
  hgvsp: ENST00000334220.4:c.231G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.*30G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.111G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.*25G>A
  variant of: http://identifiers.org/hgnc/2911
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8489
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12474
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6817
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg10His
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum

14-75356019-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75356019
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75356019
    reference: chr 14
allele count: 1
allele frequency: 8.274446853227862e-6
allele num: 120854
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.144T>G
  hgvsp: ENSP00000451425.1:p.Ser49Ala
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.*40T>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.241T>G
  hgvsp: ENSP00000335304.4:p.Ser81Ala
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.207T>G
  hgvsp: ENSP00000452417.1:p.Asn69Lys
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.183T>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.241T>G
  hgvsp: ENSP00000451210.1:p.Ser81Ala
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.190T>G
  hgvsp: ENSP00000451957.1:p.Ser64Ala
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.*35T>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.190T>G
  hgvsp: ENSP00000452422.1:p.Ser64Ala
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.245T>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.187T>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.273T>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.121T>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.39T>G
  hgvsp: ENSP00000335465.6:p.Asn13Lys
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.281T>G
  variant of: http://identifiers.org/hgnc/2911
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8081
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8487
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser81Ala
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

14-75356030-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75356030
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75356030
    reference: chr 14
allele count: 1
allele frequency: 8.282670995742708e-6
allele num: 120734
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.*46G>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.201G>C
  hgvsp: ENSP00000451957.1:p.Glu67Asp
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.50G>C
  hgvsp: ENSP00000335465.6:p.Arg17Thr
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.194G>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.132G>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.284G>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.155G>C
  hgvsp: ENSP00000451425.1:p.Glu52Asp
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.252G>C
  hgvsp: ENSP00000451210.1:p.Glu84Asp
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.201G>C
  hgvsp: ENSP00000452422.1:p.Glu67Asp
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.218G>C
  hgvsp: ENSP00000452417.1:p.Arg73Thr
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.252G>C
  hgvsp: ENSP00000335304.4:p.Glu84Asp
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.292G>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.*51G>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.198G>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.256G>C
  variant of: http://identifiers.org/hgnc/2911
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12939
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4111
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8490
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5790
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu84Asp
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff

14-75356042-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75356042
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75356042
    reference: chr 14
allele count: 1
allele frequency: 8.306613725848521e-6
allele num: 120386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.213G>A
  hgvsp: ENST00000555089.1:c.213G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.144G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.296G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.*63G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.62G>A
  hgvsp: ENSP00000335465.6:p.Gly21Asp
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.268G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.230G>A
  hgvsp: ENSP00000452417.1:p.Gly77Asp
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.264G>A
  hgvsp: ENST00000556460.1:c.264G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.167G>A
  hgvsp: ENST00000555988.1:c.167G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.264G>A
  hgvsp: ENST00000334220.4:c.264G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.206G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.210G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.304G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.213G>A
  hgvsp: ENST00000554806.1:c.213G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.*58G>A
  variant of: http://identifiers.org/hgnc/2911
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3005
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4108
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8488
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3669
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly21Asp
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

14-75356057-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75356057
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75356057
    reference: chr 14
allele count: 1
allele frequency: 8.660408078428655e-6
allele num: 115468
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.*68+5G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.216+5G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.274+5G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.319G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.240+5G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.159G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.278+5G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.72+5G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.223+5G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.223+5G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.220+5G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.274+5G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.306+5G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.*73+5G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.177+5G>A
  variant of: http://identifiers.org/hgnc/2911
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6761
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3351
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6372
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9992
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.274+5G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

14-75356058-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75356058
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75356058
    reference: chr 14
allele count: 2
allele frequency: 1.723098130438528e-5
allele num: 116070
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.216+6A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.274+6A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.278+6A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.306+6A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.220+6A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.177+6A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.72+6A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.223+6A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.*68+6A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.*73+6A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.240+6A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.320A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.160A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.223+6A>G
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.274+6A>G
  variant of: http://identifiers.org/hgnc/2911
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7021
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7623
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3787
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6098
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.274+6A>G
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

14-75356059-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75356059
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75356059
    reference: chr 14
allele count: 2
allele frequency: 1.752049898381106e-5
allele num: 114152
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.274+7T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.*73+7T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.306+7T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.223+7T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.*68+7T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.223+7T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.240+7T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.278+7T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.274+7T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.161T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.321T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.216+7T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.220+7T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.72+7T>C
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.177+7T>C
  variant of: http://identifiers.org/hgnc/2911
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6240
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3545
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10274
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1970
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4978
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.274+7T>C
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff

14-75356062-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75356062
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75356062
    reference: chr 14
allele count: 4
allele frequency: 3.67728175332794e-5
allele num: 108776
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.240+10A>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.220+10A>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.*73+10A>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.324A>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.223+10A>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.177+10A>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.72+10A>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.216+10A>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.*68+10A>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.164A>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.223+10A>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.278+10A>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.274+10A>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.306+10A>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.274+10A>T
  variant of: http://identifiers.org/hgnc/2911
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11553
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9815
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5394
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3021
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4651
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6899
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP

14-75356063-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75356063
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75356063
    reference: chr 14
allele count: 1
allele frequency: 9.412650602409639e-6
allele num: 106240
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.274+11G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.240+11G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.274+11G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.*73+11G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.177+11G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.220+11G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.325G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.223+11G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.72+11G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.216+11G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.165G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.306+11G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.*68+11G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.278+11G>A
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.223+11G>A
  variant of: http://identifiers.org/hgnc/2911
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4068
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11597
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5019
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4736
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3193
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8162
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9562
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

14-75356063-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75356063
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75356063
    reference: chr 14
allele count: 4
allele frequency: 3.765060240963856e-5
allele num: 106240
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.325G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.*68+11G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.*73+11G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.223+11G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.306+11G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.274+11G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.177+11G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.165G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.72+11G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.223+11G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.278+11G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.216+11G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.240+11G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.220+11G>T
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.274+11G>T
  variant of: http://identifiers.org/hgnc/2911
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5019
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1685
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2736
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11597
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4068
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3193
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

14-75356065-TTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75356065
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75356063
    reference: chr 14
allele count: 1
allele frequency: 1.014445706865769e-5
allele num: 98576
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.72+14_72+15delTC
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.278+14_278+15delTC
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.*68+14_*68+15delTC
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.306+14_306+15delTC
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.274+14_274+15delTC
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.328_329delTC
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.*73+14_*73+15delTC
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.223+14_223+15delTC
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.216+14_216+15delTC
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.274+14_274+15delTC
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.168_169delTC
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.220+14_220+15delTC
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.223+14_223+15delTC
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.240+14_240+15delTC
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.177+14_177+15delTC
  variant of: http://identifiers.org/hgnc/2911
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4018
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3629
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9100
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9495
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6374
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: TTC
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

14-75356068-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75356068
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75356069
    reference: chr 14
allele count: 114
allele frequency: 1.430758804186852e-3
allele num: 79678
alternate allele: CT
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.274+17dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.331dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.240+17dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.278+17dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.306+17dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.177+17dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.274+17dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.*73+17dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.171dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.72+17dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.*68+17dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.220+17dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.223+17dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.216+17dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.223+17dupT
  variant of: http://identifiers.org/hgnc/2911
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 10551
  bin: 2.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2678
  bin: 4.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 3997
  bin: 3.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6590
  bin: 1.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 9.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 6347
  bin: 3.25e1
  variant carriers: 11
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD

14-75356068-C-CTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75356068
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75356070
    reference: chr 14
allele count: 43
allele frequency: 5.396721805266196e-4
allele num: 79678
alternate allele: CTT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.306+17_306+18insTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.331_332insTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.*73+17_*73+18insTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.240+17_240+18insTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.72+17_72+18insTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.171_172insTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.274+17_274+18insTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.274+17_274+18insTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.220+17_220+18insTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.223+17_223+18insTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.223+17_223+18insTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.278+17_278+18insTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.177+17_177+18insTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.216+17_216+18insTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.*68+17_*68+18insTT
  variant of: http://identifiers.org/hgnc/2911
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 10551
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6347
  bin: 3.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 9455
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD

14-75356068-C-CTTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75356068
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75356071
    reference: chr 14
allele count: 3
allele frequency: 3.765154747860137e-5
allele num: 79678
alternate allele: CTTT
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.223+17_223+18insTTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.240+17_240+18insTTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.*73+17_*73+18insTTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.216+17_216+18insTTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.220+17_220+18insTTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.274+17_274+18insTTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.171_172insTTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.331_332insTTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.*68+17_*68+18insTTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.223+17_223+18insTTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.177+17_177+18insTTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.306+17_306+18insTTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.72+17_72+18insTTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.274+17_274+18insTTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.278+17_278+18insTTT
  variant of: http://identifiers.org/hgnc/2911
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 3750
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9094
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9455
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6590
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2678
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD

14-75356068-C-CTTTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75356068
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75356072
    reference: chr 14
allele count: 2
allele frequency: 2.510103165240091e-5
allele num: 79678
alternate allele: CTTTT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.171_172insTTTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.240+17_240+18insTTTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.331_332insTTTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.278+17_278+18insTTTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.274+17_274+18insTTTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.177+17_177+18insTTTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.216+17_216+18insTTTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.*68+17_*68+18insTTTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.274+17_274+18insTTTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.223+17_223+18insTTTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.220+17_220+18insTTTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.*73+17_*73+18insTTTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.223+17_223+18insTTTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.306+17_306+18insTTTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.72+17_72+18insTTTT
  variant of: http://identifiers.org/hgnc/2911
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 9455
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3997
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6590
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6347
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2678
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

14-75356068-CTA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75356068
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75356066
    reference: chr 14
allele count: 9
allele frequency: 1.129546424358041e-4
allele num: 79678
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.306+18_306+19delAT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.177+18_177+19delAT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.*68+18_*68+19delAT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.72+18_72+19delAT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.216+18_216+19delAT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.223+18_223+19delAT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.240+18_240+19delAT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.278+18_278+19delAT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.172_173delAT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.332_333delAT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.223+18_223+19delAT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.*73+18_*73+19delAT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.220+18_220+19delAT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.274+18_274+19delAT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.274+18_274+19delAT
  variant of: http://identifiers.org/hgnc/2911
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 3750
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9094
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6347
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6590
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9455
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10551
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3997
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: CTA
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum

14-75356068-CTAT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75356068
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75356065
    reference: chr 14
allele count: 5
allele frequency: 6.275257913100228e-5
allele num: 79678
alternate allele: C
canonical: false
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 10551
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2678
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6590
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6347
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3750
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3997
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9094
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9455
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7085
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4771
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6220
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10364
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3402
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2081
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 610
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3577
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2645
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5987
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4654
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2430
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1170
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1363
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 503
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2014
  bin: 9.75e1
  variant carriers: 5
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 5868
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 10368
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 4
  allele frequency: 8.700191404210893e-5
  allele num: 45976
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4532
  num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
reference allele: CTAT
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

14-75356069-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75356069
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75356068
    reference: chr 14
allele count: 61
allele frequency: 8.227899322884351e-4
allele num: 74138
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.274+18delA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.278+18delA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.177+18delA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.*68+18delA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.216+18delA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.220+18delA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.332delA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.72+18delA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.240+18delA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.172delA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.223+18delA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.*73+18delA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.274+18delA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.306+18delA
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.223+18delA
  variant of: http://identifiers.org/hgnc/2911
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 1664
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6289
  bin: 3.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 6630
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2666
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8853
  bin: 2.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: TA
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ

14-75356070-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75356070
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75356071
    reference: chr 14
allele count: 1476
allele frequency: 8.141202426916713e-2
allele num: 18130
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.220+38dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.216+38dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.274+38dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.278+38dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.306+38dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.274+38dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.352dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.192dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.240+38dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.*68+38dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.177+38dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.*73+38dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.72+38dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.223+38dupT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.223+38dupT
  variant of: http://identifiers.org/hgnc/2911
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 4.25e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 5.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 3052
  bin: 3.75e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 2.5e0
  variant carriers: 457
genotype depth: GenotypeDepth
  all individuals: 7728
  bin: 2.75e1
  variant carriers: 149
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 5.75e1
  variant carriers: 28
genotype quality: GenotypeQuality
num of homozygotes: 71
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ

14-75356070-A-ATT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75356070
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75356072
    reference: chr 14
allele count: 437
allele frequency: 2.410369553226696e-2
allele num: 18130
alternate allele: ATT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.306+37_306+38dupTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.*73+37_*73+38dupTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.240+37_240+38dupTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.216+37_216+38dupTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.177+37_177+38dupTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.223+37_223+38dupTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.223+37_223+38dupTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.351_352dupTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.278+37_278+38dupTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.191_192dupTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.72+37_72+38dupTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.220+37_220+38dupTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.274+37_274+38dupTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.274+37_274+38dupTT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.*68+37_*68+38dupTT
  variant of: http://identifiers.org/hgnc/2911
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9338
  bin: 1.25e1
  variant carriers: 244
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7281
  bin: 7.5e0
  variant carriers: 487
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 2.5e0
  variant carriers: 110
genotype depth: GenotypeDepth
  all individuals: 9983
  bin: 2.25e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 5026
  bin: 3.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 5.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 3052
  bin: 3.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 15
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

14-75356070-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75356070
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75356070
    reference: chr 14
allele count: 828
allele frequency: 4.567015995587424e-2
allele num: 18130
alternate allele: T
canonical: false
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5026
  bin: 3.25e1
  variant carriers: 107
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 4.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 9.75e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 9983
  bin: 2.25e1
  variant carriers: 160
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 4.25e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 9338
  bin: 1.25e1
  variant carriers: 74
genotype depth: GenotypeDepth
  all individuals: 3052
  bin: 3.75e1
  variant carriers: 83
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 7728
  bin: 2.75e1
  variant carriers: 128
genotype depth: GenotypeDepth
  all individuals: 7281
  bin: 7.5e0
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 5.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 5.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 10070
  bin: 1.75e1
  variant carriers: 121
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 903
  bin: 4.25e1
  variant carriers: 24
genotype quality: GenotypeQuality
  all individuals: 1584
  bin: 2.25e1
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 1437
  bin: 1.75e1
  variant carriers: 29
genotype quality: GenotypeQuality
  all individuals: 3047
  bin: 7.5e0
  variant carriers: 33
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 7.75e1
  variant carriers: 24
genotype quality: GenotypeQuality
  all individuals: 493
  bin: 6.25e1
  variant carriers: 24
genotype quality: GenotypeQuality
  all individuals: 1770
  bin: 1.25e1
  variant carriers: 38
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 8.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 1061
  bin: 3.25e1
  variant carriers: 29
genotype quality: GenotypeQuality
  all individuals: 1376
  bin: 9.75e1
  variant carriers: 486
genotype quality: GenotypeQuality
  all individuals: 986
  bin: 3.75e1
  variant carriers: 36
genotype quality: GenotypeQuality
  all individuals: 666
  bin: 5.25e1
  variant carriers: 25
genotype quality: GenotypeQuality
  all individuals: 785
  bin: 4.75e1
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 1131
  bin: 2.75e1
  variant carriers: 36
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 7.25e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 41772
  bin: 2.5e0
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 6.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 9.25e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 556
  bin: 5.75e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 8.25e1
  variant carriers: 13
num of homozygotes: 2
population: European (Finnish)
  type: Population
  allele count: 52
  allele frequency: 4.05616224648986e-2
  allele num: 1282
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 41
  allele frequency: 3.264331210191083e-2
  allele num: 1256
  num of homozygotes: 0
population: African
  type: Population
  allele count: 86
  allele frequency: 5.850340136054422e-2
  allele num: 1470
  num of homozygotes: 1
population: South Asian
  type: Population
  allele count: 128
  allele frequency: 7.950310559006211e-2
  allele num: 1610
  num of homozygotes: 1
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

14-75356070-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75356070
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 75356069
    reference: chr 14
allele count: 2608
allele frequency: 1.43849972421401e-1
allele num: 18130
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451210
  ensembl transcript: ENST00000556460
  gene symbol: DLST
  hgvsc: ENST00000556460.1:c.274+38delT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555071
  gene symbol: DLST
  hgvsc: ENST00000555071.1:n.306+38delT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555190
  gene symbol: DLST
  hgvsc: ENST00000555190.1:n.220+38delT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452417
  ensembl transcript: ENST00000555492
  gene symbol: DLST
  hgvsc: ENST00000555492.1:c.240+38delT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451957
  ensembl transcript: ENST00000554806
  gene symbol: DLST
  hgvsc: ENST00000554806.1:c.223+38delT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335304
  ensembl transcript: ENST00000334220
  gene symbol: DLST
  hgvsc: ENST00000334220.4:c.274+38delT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000557012
  gene symbol: DLST
  hgvsc: ENST00000557012.1:n.352delT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000452422
  ensembl transcript: ENST00000555089
  gene symbol: DLST
  hgvsc: ENST00000555089.1:c.223+38delT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000238671
  ensembl transcript: ENST00000238671
  gene symbol: DLST
  hgvsc: ENST00000238671.7:c.*68+38delT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000550473
  gene symbol: DLST
  hgvsc: ENST00000550473.2:n.192delT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451425
  ensembl transcript: ENST00000555988
  gene symbol: DLST
  hgvsc: ENST00000555988.1:c.177+38delT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000335465
  ensembl transcript: ENST00000334212
  gene symbol: DLST
  hgvsc: ENST00000334212.6:c.72+38delT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000555459
  gene symbol: DLST
  hgvsc: ENST00000555459.1:n.216+38delT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl protein: ENSP00000451670
  ensembl transcript: ENST00000554612
  gene symbol: DLST
  hgvsc: ENST00000554612.1:c.*73+38delT
  variant of: http://identifiers.org/hgnc/2911
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000119689
  ensembl transcript: ENST00000556582
  gene symbol: DLST
  hgvsc: ENST00000556582.1:n.278+38delT
  variant of: http://identifiers.org/hgnc/2911
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 2.5e0
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 7728
  bin: 2.75e1
  variant carriers: 169
genotype depth: GenotypeDepth
  all individuals: 7281
  bin: 7.5e0
  variant carriers: 1026
genotype depth: GenotypeDepth
  all individuals: 5026
  bin: 3.25e1
  variant carriers: 104
genotype depth: GenotypeDepth
  all individuals: 3052
  bin: 3.75e1
  variant carriers: 96
genotype depth: GenotypeDepth
  all individuals: 9338
  bin: 1.25e1
  variant carriers: 1458
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 4.25e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 5.75e1
  variant carriers: 36
genotype quality: GenotypeQuality
num of homozygotes: 0
reference allele: AT

GenotypeDepth
all individuals: 1670
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 124
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 533
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 843
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7848
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1939
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 510
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 649
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 392
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11728
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2493
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 132
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2755
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 862
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1362
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11235
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4960
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1847
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16409
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1310
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3058
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 624
bin: 4.75e1
variant carriers: 0

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

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

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.16827041697508e-5
allele num: 16212
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66244
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -6.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.833e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.2e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.28e-1

MQ
type: SiteQuality
SIO_000300: 6.027e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

QD
type: SiteQuality
SIO_000300: 1.065e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -3.41e-1

DP
type: SiteQuality
SIO_000300: 3.585767e6

GenotypeDepth
all individuals: 13
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 100
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4937
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 402
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7385
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5286
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6703
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16411
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2735
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 660
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5403
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8919
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2918
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1705
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1538
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1079
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1639
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 561
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5922
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1363
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 733
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1706
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3285
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1080
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2492
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10714
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.688789813219847e-5
allele num: 59214
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12340
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7966
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5670
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 750
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7902
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.664073e6

VQSLOD
type: SiteQuality
SIO_000300: 7.6e-2

QD
type: SiteQuality
SIO_000300: 1.363e1

MQRankSum
type: SiteQuality
SIO_000300: -8.91e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.295e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.37e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.71e-1

MQ
type: SiteQuality
SIO_000300: 5.997e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.2e-3

GenotypeDepth
all individuals: 84
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7666
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5422
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5127
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 568
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 343
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6675
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2476
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2873
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2706
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4209
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1124
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1174
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2865
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 605
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 867
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5039
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1360
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 817
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2984
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7023
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1606
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3144
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1271
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16401
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52270
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9584
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7180
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9964
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 622
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.006420545746388e-4
allele num: 4984
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4528
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.1e-2

QD
type: SiteQuality
SIO_000300: 1.482e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.21e-2

MQRankSum
type: SiteQuality
SIO_000300: -5.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.16e0

DP
type: SiteQuality
SIO_000300: 3.752965e6

FS
type: SiteQuality
SIO_000300: 1.4942e1

VQSLOD
type: SiteQuality
SIO_000300: -1.01e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 7

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

GenotypeQuality
all individuals: 188
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GenotypeQuality
all individuals: 730
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8874
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 534
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9100
num of homozygotes: 0

African
type: Population
allele count: 23
allele frequency: 1.266519823788546e-2
allele num: 1816
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46912
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3690
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6680
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.409e1

MQ
type: SiteQuality
SIO_000300: 5.981e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.59e0

DP
type: SiteQuality
SIO_000300: 3.903084e6

FS
type: SiteQuality
SIO_000300: 6.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.33e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.29e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.14e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.08e0

GenotypeDepth
all individuals: 2690
bin: 8.25e1
variant carriers: 2589

GenotypeDepth
all individuals: 8294
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variant carriers: 7499

GenotypeDepth
all individuals: 4
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variant carriers: 0

GenotypeDepth
all individuals: 4266
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variant carriers: 2666

GenotypeDepth
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variant carriers: 153

GenotypeDepth
all individuals: 5105
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variant carriers: 4722

GenotypeDepth
all individuals: 1364
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variant carriers: 1296

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 3

GenotypeQuality
all individuals: 21
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variant carriers: 7

GenotypeQuality
all individuals: 4
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variant carriers: 3

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 7

GenotypeQuality
all individuals: 31
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variant carriers: 9

GenotypeQuality
all individuals: 557
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variant carriers: 30

GenotypeQuality
all individuals: 11
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variant carriers: 2

GenotypeQuality
all individuals: 592
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variant carriers: 56

GenotypeQuality
all individuals: 10
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variant carriers: 1

GenotypeQuality
all individuals: 35
bin: 5.25e1
variant carriers: 17

GenotypeQuality
all individuals: 468
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variant carriers: 140

GenotypeQuality
all individuals: 36
bin: 4.75e1
variant carriers: 16

GenotypeQuality
all individuals: 389
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variant carriers: 51

GenotypeQuality
all individuals: 56442
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variant carriers: 48767

GenotypeQuality
all individuals: 607
bin: 7.75e1
variant carriers: 80

GenotypeQuality
all individuals: 780
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variant carriers: 173

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 2

GenotypeQuality
all individuals: 635
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variant carriers: 41

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 15

South Asian
type: Population
allele count: 10982
allele frequency: 6.651726226529376e-1
allele num: 16510
num of homozygotes: 3707

European (Non-Finnish)
type: Population
allele count: 36294
allele frequency: 5.441542475036732e-1
allele num: 66698
num of homozygotes: 9914

East Asian
type: Population
allele count: 4084
allele frequency: 4.720295885344429e-1
allele num: 8652
num of homozygotes: 990

Other
type: Population
allele count: 569
allele frequency: 6.280353200883002e-1
allele num: 906
num of homozygotes: 186

Latino
type: Population
allele count: 5581
allele frequency: 4.828690084789756e-1
allele num: 11558
num of homozygotes: 1350

European (Finnish)
type: Population
allele count: 4364
allele frequency: 6.606115652437178e-1
allele num: 6606
num of homozygotes: 1457

African
type: Population
allele count: 9454
allele frequency: 9.092133102519715e-1
allele num: 10398
num of homozygotes: 4318

ClippingRankSum
type: SiteQuality
SIO_000300: -4.58e-1

MQ
type: SiteQuality
SIO_000300: 6.032e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.2e-2

DP
type: SiteQuality
SIO_000300: 4.551731e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.12e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.53e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.999999999999999e-3

QD
type: SiteQuality
SIO_000300: 2.249e1

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

GenotypeDepth
all individuals: 4
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variant carriers: 0

GenotypeDepth
all individuals: 856
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variant carriers: 0

GenotypeDepth
all individuals: 800
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variant carriers: 0

GenotypeDepth
all individuals: 329
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variant carriers: 0

GenotypeDepth
all individuals: 2114
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variant carriers: 0

GenotypeDepth
all individuals: 2422
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variant carriers: 0

GenotypeQuality
all individuals: 619
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variant carriers: 0

GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
all individuals: 533
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 331
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GenotypeQuality
all individuals: 341
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GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 20889
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GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 609
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GenotypeQuality
all individuals: 21
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GenotypeQuality
all individuals: 534
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GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7678
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variant carriers: 1

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 522
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13942
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1960
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3104
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 790
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 140
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 4.068348250610252e-4
allele num: 2458
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 128
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.71e0

VQSLOD
type: SiteQuality
SIO_000300: 8.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.833e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.83e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.0e-2

DP
type: SiteQuality
SIO_000300: 4.722783e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.65e-1

QD
type: SiteQuality
SIO_000300: 1.69e1

MQ
type: SiteQuality
SIO_000300: 6.02e1

FS
type: SiteQuality
SIO_000300: 6.518e0

GenotypeDepth
all individuals: 4
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variant carriers: 0

GenotypeDepth
all individuals: 10
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variant carriers: 0

GenotypeDepth
all individuals: 6737
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 5749
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variant carriers: 0

GenotypeDepth
all individuals: 2497
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 1
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GenotypeQuality
all individuals: 19
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GenotypeQuality
all individuals: 46134
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GenotypeQuality
all individuals: 2234
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GenotypeQuality
all individuals: 4
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GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 6
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GenotypeQuality
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GenotypeQuality
all individuals: 0
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GenotypeQuality
all individuals: 20
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GenotypeQuality
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GenotypeQuality
all individuals: 25
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GenotypeQuality
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GenotypeQuality
all individuals: 1311
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GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 1269
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GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 2091
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variant carriers: 0

GenotypeQuality
all individuals: 2559
bin: 9.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.59e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.86e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.53e0

FS
type: SiteQuality
SIO_000300: 4.46e0

QD
type: SiteQuality
SIO_000300: 1.647e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.89e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.095e0

DP
type: SiteQuality
SIO_000300: 3.939088e6

MQRankSum
type: SiteQuality
SIO_000300: 1.41e0

MQ
type: SiteQuality
SIO_000300: 6.039e1

GenotypeDepth
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6736
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variant carriers: 0

GenotypeDepth
all individuals: 6288
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1193
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variant carriers: 0

GenotypeDepth
all individuals: 811
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variant carriers: 0

GenotypeDepth
all individuals: 2497
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variant carriers: 2

GenotypeDepth
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 2225
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GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 15
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GenotypeQuality
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GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 29
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 21
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 26
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999220202747286e-5
allele num: 66684
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.049e1

MQRankSum
type: SiteQuality
SIO_000300: -3.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.3e-2

DP
type: SiteQuality
SIO_000300: 3.939082e6

FS
type: SiteQuality
SIO_000300: 1.909e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.44e0

VQSLOD
type: SiteQuality
SIO_000300: 1.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

QD
type: SiteQuality
SIO_000300: 1.294e1

GenotypeDepth
all individuals: 5746
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variant carriers: 2

GenotypeDepth
all individuals: 6727
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variant carriers: 2

GenotypeDepth
all individuals: 3
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variant carriers: 0

GenotypeDepth
all individuals: 6511
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variant carriers: 2

GenotypeDepth
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GenotypeDepth
all individuals: 2496
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GenotypeDepth
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GenotypeDepth
all individuals: 809
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GenotypeDepth
all individuals: 1191
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GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 2830
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GenotypeQuality
all individuals: 4
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GenotypeQuality
all individuals: 1
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GenotypeQuality
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GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 8
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GenotypeQuality
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GenotypeQuality
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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: 46078
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2552
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GenotypeQuality
all individuals: 7
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 2.098006893451221e-4
allele num: 66730
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 10
allele frequency: 6.056935190793458e-4
allele num: 16510
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.45e-1

MQ
type: SiteQuality
SIO_000300: 6.013e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.4e-2

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 3.939051e6

FS
type: SiteQuality
SIO_000300: 2.812e0

QD
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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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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European (Finnish)
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MQRankSum
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FS
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MQ
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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QD
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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East Asian
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South Asian
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European (Finnish)
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QD
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VQSLOD
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MQRankSum
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FS
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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DP
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MQ
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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Other
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East Asian
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African
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MQ
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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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QD
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ClippingRankSum
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DP
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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Other
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African
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Latino
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East Asian
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European (Non-Finnish)
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VQSLOD
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FS
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ReadPosRankSum
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MQRankSum
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DP
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BaseQRankSum
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QD
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ClippingRankSum
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InbreedingCoeff
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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Latino
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European (Finnish)
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African
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East Asian
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South Asian
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European (Non-Finnish)
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MQRankSum
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MQ
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DP
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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FS
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VQSLOD
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QD
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BaseQRankSum
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GenotypeQuality
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African
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South Asian
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European (Finnish)
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East Asian
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FS
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DP
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ReadPosRankSum
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InbreedingCoeff
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SIO_000300: 0.0e0

BaseQRankSum
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VQSLOD
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MQRankSum
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SIO_000300: -1.345e0

MQ
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SIO_000300: 6.053e1

ClippingRankSum
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SIO_000300: -1.551e0

QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
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num of homozygotes: 0

Latino
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Other
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South Asian
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East Asian
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African
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QD
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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FS
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MQ
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DP
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Finnish)
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European (Non-Finnish)
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African
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East Asian
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South Asian
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BaseQRankSum
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VQSLOD
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QD
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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FS
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ReadPosRankSum
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DP
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MQ
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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South Asian
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Latino
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Other
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European (Finnish)
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East Asian
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MQRankSum
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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FS
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MQ
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DP
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QD
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ReadPosRankSum
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GenotypeQuality
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European (Finnish)
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South Asian
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African
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Latino
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European (Non-Finnish)
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Other
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QD
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MQ
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MQRankSum
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DP
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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FS
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BaseQRankSum
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GenotypeQuality
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European (Non-Finnish)
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BaseQRankSum
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QD
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InbreedingCoeff
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FS
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MQ
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MQRankSum
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DP
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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European (Finnish)
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African
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Latino
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DP
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MQ
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InbreedingCoeff
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VQSLOD
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GenotypeQuality
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European (Finnish)
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Latino
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East Asian
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European (Non-Finnish)
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South Asian
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MQRankSum
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ReadPosRankSum
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MQ
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QD
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DP
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ClippingRankSum
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BaseQRankSum
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FS
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VQSLOD
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InbreedingCoeff
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East Asian
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European (Non-Finnish)
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European (Finnish)
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South Asian
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African
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FS
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QD
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DP
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ReadPosRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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MQ
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African
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European (Finnish)
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MQ
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DP
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FS
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VQSLOD
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Other
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.498845888665727e-5
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num of homozygotes: 0

InbreedingCoeff
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ReadPosRankSum
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FS
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BaseQRankSum
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MQ
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MQRankSum
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QD
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ClippingRankSum
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VQSLOD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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Other
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South Asian
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European (Finnish)
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European (Non-Finnish)
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East Asian
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ClippingRankSum
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DP
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MQRankSum
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BaseQRankSum
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FS
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MQ
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VQSLOD
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InbreedingCoeff
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QD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele num: 6614
num of homozygotes: 0

African
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allele num: 10338
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East Asian
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num of homozygotes: 0

Latino
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allele frequency: 3.455425017277125e-4
allele num: 11576
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Other
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European (Non-Finnish)
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allele frequency: 1.993943210098648e-3
allele num: 66702
num of homozygotes: 0

South Asian
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ClippingRankSum
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MQ
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DP
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VQSLOD
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FS
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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QD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

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

Latino
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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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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.513225591671206e-5
allele num: 66084
num of homozygotes: 0

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

East Asian
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South Asian
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African
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Latino
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Other
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European (Non-Finnish)
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MQRankSum
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ReadPosRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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QD
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BaseQRankSum
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VQSLOD
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MQ
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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South Asian
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African
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Latino
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East Asian
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European (Non-Finnish)
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QD
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MQRankSum
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MQ
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ClippingRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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Latino
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South Asian
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East Asian
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European (Non-Finnish)
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MQ
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FS
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BaseQRankSum
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VQSLOD
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QD
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InbreedingCoeff
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DP
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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allele frequency: 1.505298651252408e-5
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num of homozygotes: 0

East Asian
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Latino
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allele frequency: 0.0e0
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African
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Other
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MQ
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QD
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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DP
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VQSLOD
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FS
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InbreedingCoeff
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

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

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

African
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allele num: 10180
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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

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

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

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

South Asian
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Other
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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
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East Asian
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European (Non-Finnish)
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allele count: 1
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allele num: 66498
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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QD
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InbreedingCoeff
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FS
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ClippingRankSum
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MQRankSum
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MQ
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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European (Non-Finnish)
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South Asian
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Latino
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European (Finnish)
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QD
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VQSLOD
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MQRankSum
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FS
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DP
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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European (Finnish)
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South Asian
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MQ
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BaseQRankSum
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InbreedingCoeff
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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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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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num of homozygotes: 0

South Asian
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East Asian
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European (Finnish)
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.505298651252408e-5
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QD
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ClippingRankSum
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VQSLOD
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FS
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MQRankSum
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MQ
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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South Asian
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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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Other
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MQ
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MQRankSum
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DP
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VQSLOD
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ClippingRankSum
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FS
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ReadPosRankSum
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BaseQRankSum
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QD
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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South Asian
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African
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East Asian
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Latino
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Other
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
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MQ
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DP
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QD
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MQRankSum
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VQSLOD
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 63264
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Latino
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South Asian
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African
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Other
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European (Finnish)
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East Asian
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ClippingRankSum
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FS
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QD
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DP
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InbreedingCoeff
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MQRankSum
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MQ
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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South Asian
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Other
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African
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European (Finnish)
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DP
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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QD
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FS
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MQ
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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European (Finnish)
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Latino
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South Asian
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QD
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BaseQRankSum
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DP
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ReadPosRankSum
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MQ
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VQSLOD
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ClippingRankSum
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FS
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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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East Asian
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 9.022013713460844e-5
allele num: 11084
num of homozygotes: 0

African
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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 frequency: 1.673024158468848e-5
allele num: 59772
num of homozygotes: 0

European (Finnish)
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allele frequency: 3.595828838547285e-4
allele num: 5562
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MQ
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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QD
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MQRankSum
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InbreedingCoeff
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FS
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 58450
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Other
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VQSLOD
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FS
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ClippingRankSum
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DP
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MQRankSum
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QD
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InbreedingCoeff
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BaseQRankSum
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MQ
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

Latino
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allele count: 1
allele frequency: 9.196247930844215e-5
allele num: 10874
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.421727972626176e-5
allele num: 58450
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.182312603452353e-4
allele num: 8458
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5790
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.3823e1

MQ
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SIO_000300: 5.635e1

InbreedingCoeff
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SIO_000300: 1.11e-2

QD
type: SiteQuality
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DP
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MQRankSum
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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SIO_000300: -8.35e-1

ReadPosRankSum
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 0
allele frequency: 0.0e0
allele num: 10068
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: 1
allele frequency: 7.255840951966333e-5
allele num: 13782
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54336
num of homozygotes: 0

Other
type: Population
allele count: 0
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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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6030
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
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SIO_000300: 5.624e1

QD
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VQSLOD
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SIO_000300: 1.85e0

InbreedingCoeff
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DP
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GenotypeDepth
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variant carriers: 3

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 1.446759259259259e-3
allele num: 10368
num of homozygotes: 0

East Asian
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Latino
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allele frequency: 7.712082262210797e-4
allele num: 7780
num of homozygotes: 0

African
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allele count: 19
allele frequency: 3.237900477164281e-3
allele num: 5868
num of homozygotes: 0

European (Non-Finnish)
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allele count: 63
allele frequency: 1.370280146163216e-3
allele num: 45976
num of homozygotes: 0

European (Finnish)
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allele frequency: 1.333333333333333e-3
allele num: 4500
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Other
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MQRankSum
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MQ
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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DP
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BaseQRankSum
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ReadPosRankSum
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FS
type: SiteQuality
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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allele count: 0
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African
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allele count: 14
allele frequency: 2.385821404226312e-3
allele num: 5868
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 1.285347043701799e-4
allele num: 7780
num of homozygotes: 0

European (Finnish)
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allele count: 2
allele frequency: 4.444444444444445e-4
allele num: 4500
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East Asian
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allele count: 1
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European (Non-Finnish)
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allele count: 24
allele frequency: 5.220114842526536e-4
allele num: 45976
num of homozygotes: 0

South Asian
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ClippingRankSum
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DP
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MQ
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FS
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MQRankSum
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QD
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1170
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4532
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.175047851052723e-5
allele num: 45976
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4500
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 3.408316291751875e-4
allele num: 5868
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7780
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.648e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.39e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.422e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.88e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.1e-2

VQSLOD
type: SiteQuality
SIO_000300: -4.274e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.444e0

DP
type: SiteQuality
SIO_000300: 1.72651e6

FS
type: SiteQuality
SIO_000300: 1.684e1

QD
type: SiteQuality
SIO_000300: 3.4e0

GenotypeDepth
all individuals: 10551
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3750
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variant carriers: 0

GenotypeDepth
all individuals: 769
bin: 5.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 1235
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9094
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variant carriers: 0

GenotypeDepth
all individuals: 179
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variant carriers: 0

GenotypeDepth
all individuals: 1155
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 2081
bin: 4.25e1
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3577
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6220
bin: 3.25e1
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GenotypeQuality
all individuals: 503
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4500
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5868
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4532
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.350095702105447e-5
allele num: 45976
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7780
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 654
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.684e1

MQRankSum
type: SiteQuality
SIO_000300: -7.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.39e0

VQSLOD
type: SiteQuality
SIO_000300: -4.274e-1

DP
type: SiteQuality
SIO_000300: 1.72651e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.444e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.422e-1

MQ
type: SiteQuality
SIO_000300: 5.648e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.1e-2

QD
type: SiteQuality
SIO_000300: 3.4e0

GenotypeDepth
all individuals: 555
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1235
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 396
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variant carriers: 0

GenotypeDepth
all individuals: 378
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variant carriers: 0

GenotypeDepth
all individuals: 196
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variant carriers: 0

GenotypeDepth
all individuals: 582
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variant carriers: 0

GenotypeDepth
all individuals: 2678
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variant carriers: 0

GenotypeDepth
all individuals: 135
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variant carriers: 0

GenotypeDepth
all individuals: 179
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 610
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5987
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 381
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3577
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7085
bin: 2.5e0
variant carriers: 2

GenotypeQuality
all individuals: 4654
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4771
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2014
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 10364
bin: 2.25e1
variant carriers: 2

GenotypeQuality
all individuals: 6220
bin: 3.25e1
variant carriers: 3

GenotypeQuality
all individuals: 2645
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variant carriers: 0

GenotypeQuality
all individuals: 503
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variant carriers: 2

GenotypeQuality
all individuals: 3402
bin: 1.25e1
variant carriers: 4

GenotypeQuality
all individuals: 2430
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variant carriers: 0

GenotypeQuality
all individuals: 200
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variant carriers: 0

GenotypeQuality
all individuals: 240
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variant carriers: 0

GenotypeQuality
all individuals: 1170
bin: 5.25e1
variant carriers: 1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1363
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 5.75e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 1.704158145875937e-4
allele num: 5868
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 654
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.285347043701799e-4
allele num: 7780
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4532
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 4
allele frequency: 8.888888888888889e-4
allele num: 4500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.52514355315817e-5
allele num: 45976
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.444e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.422e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.39e0

VQSLOD
type: SiteQuality
SIO_000300: -4.274e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.88e-1

FS
type: SiteQuality
SIO_000300: 1.684e1

MQ
type: SiteQuality
SIO_000300: 5.648e1

QD
type: SiteQuality
SIO_000300: 3.4e0

DP
type: SiteQuality
SIO_000300: 1.72651e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.1e-2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4500
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.285347043701799e-4
allele num: 7780
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 654
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.444e0

MQRankSum
type: SiteQuality
SIO_000300: -7.88e-1

FS
type: SiteQuality
SIO_000300: 1.684e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.422e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.274e-1

MQ
type: SiteQuality
SIO_000300: 5.648e1

QD
type: SiteQuality
SIO_000300: 3.4e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.39e0

DP
type: SiteQuality
SIO_000300: 1.72651e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.1e-2

GenotypeDepth
all individuals: 597
bin: 2.5e0
variant carriers: 1

GenotypeDepth
all individuals: 3937
bin: 3.75e1
variant carriers: 9

GenotypeDepth
all individuals: 3844
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 240
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 130
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9548
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variant carriers: 10

GenotypeDepth
all individuals: 1233
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variant carriers: 2

GenotypeDepth
all individuals: 381
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variant carriers: 0

GenotypeDepth
all individuals: 10532
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variant carriers: 15

GenotypeQuality
all individuals: 7998
bin: 2.5e0
variant carriers: 7

GenotypeQuality
all individuals: 5933
bin: 3.25e1
variant carriers: 7

GenotypeQuality
all individuals: 4349
bin: 2.75e1
variant carriers: 5

GenotypeQuality
all individuals: 2132
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2806
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variant carriers: 3

GenotypeQuality
all individuals: 4620
bin: 3.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1937
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variant carriers: 1

GenotypeQuality
all individuals: 1586
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variant carriers: 3

GenotypeQuality
all individuals: 417
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variant carriers: 3

GenotypeQuality
all individuals: 3640
bin: 1.25e1
variant carriers: 4

GenotypeQuality
all individuals: 5623
bin: 7.5e0
variant carriers: 6

GenotypeQuality
all individuals: 8247
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variant carriers: 9

GenotypeQuality
all individuals: 5338
bin: 1.75e1
variant carriers: 5

GenotypeQuality
all individuals: 381
bin: 8.25e1
variant carriers: 3

GenotypeQuality
all individuals: 177
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 249
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 584
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1941
bin: 9.75e1
variant carriers: 16

GenotypeQuality
all individuals: 763
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 991
bin: 6.75e1
variant carriers: 3

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3642
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 8.486082824168364e-4
allele num: 5892
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 13
allele frequency: 3.426462836056932e-3
allele num: 3794
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 33
allele frequency: 7.79331192140563e-4
allele num: 42344
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 3.685956505713233e-4
allele num: 10852
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 8.583690987124463e-4
allele num: 6990
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 624
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.1082e1

QD
type: SiteQuality
SIO_000300: 1.21e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.070000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.25e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.27e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

DP
type: SiteQuality
SIO_000300: 1.710248e6

MQRankSum
type: SiteQuality
SIO_000300: -4.27e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.384e0

MQ
type: SiteQuality
SIO_000300: 5.678e1

GenotypeDepth
all individuals: 7281
bin: 7.5e0
variant carriers: 1929

GenotypeDepth
all individuals: 9983
bin: 2.25e1
variant carriers: 185

GenotypeDepth
all individuals: 10070
bin: 1.75e1
variant carriers: 372

GenotypeDepth
all individuals: 5026
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variant carriers: 63

GenotypeDepth
all individuals: 9338
bin: 1.25e1
variant carriers: 989

GenotypeDepth
all individuals: 152
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variant carriers: 6

GenotypeDepth
all individuals: 1241
bin: 4.75e1
variant carriers: 38

GenotypeDepth
all individuals: 70
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variant carriers: 2

GenotypeDepth
all individuals: 97
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variant carriers: 3

GenotypeQuality
all individuals: 1061
bin: 3.25e1
variant carriers: 291

GenotypeQuality
all individuals: 219
bin: 8.75e1
variant carriers: 25

GenotypeQuality
all individuals: 556
bin: 5.75e1
variant carriers: 87

GenotypeQuality
all individuals: 41772
bin: 2.5e0
variant carriers: 553

GenotypeQuality
all individuals: 1437
bin: 1.75e1
variant carriers: 438

GenotypeQuality
all individuals: 785
bin: 4.75e1
variant carriers: 158

GenotypeQuality
all individuals: 1584
bin: 2.25e1
variant carriers: 397

GenotypeQuality
all individuals: 304
bin: 7.75e1
variant carriers: 41

GenotypeQuality
all individuals: 666
bin: 5.25e1
variant carriers: 142

GenotypeQuality
all individuals: 3047
bin: 7.5e0
variant carriers: 531

GenotypeQuality
all individuals: 1131
bin: 2.75e1
variant carriers: 348

GenotypeQuality
all individuals: 986
bin: 3.75e1
variant carriers: 262

GenotypeQuality
all individuals: 903
bin: 4.25e1
variant carriers: 227

GenotypeQuality
all individuals: 1770
bin: 1.25e1
variant carriers: 503

GenotypeQuality
all individuals: 247
bin: 8.25e1
variant carriers: 28

GenotypeQuality
all individuals: 1376
bin: 9.75e1
variant carriers: 124

GenotypeQuality
all individuals: 464
bin: 6.75e1
variant carriers: 70

GenotypeQuality
all individuals: 354
bin: 7.25e1
variant carriers: 43

GenotypeQuality
all individuals: 211
bin: 9.25e1
variant carriers: 22

GenotypeQuality
all individuals: 493
bin: 6.25e1
variant carriers: 88

Latino
type: Population
allele count: 80
allele frequency: 6.369426751592357e-2
allele num: 1256
num of homozygotes: 3

East Asian
type: Population
allele count: 59
allele frequency: 7.412060301507538e-2
allele num: 796
num of homozygotes: 3

Other
type: Population
allele count: 15
allele frequency: 9.49367088607595e-2
allele num: 158
num of homozygotes: 0

African
type: Population
allele count: 192
allele frequency: 1.306122448979592e-1
allele num: 1470
num of homozygotes: 20

European (Non-Finnish)
type: Population
allele count: 867
allele frequency: 7.501297802387956e-2
allele num: 11558
num of homozygotes: 21

European (Finnish)
type: Population
allele count: 100
allele frequency: 7.800312012480499e-2
allele num: 1282
num of homozygotes: 1

South Asian
type: Population
allele count: 163
allele frequency: 1.012422360248447e-1
allele num: 1610
num of homozygotes: 23

ClippingRankSum
type: SiteQuality
SIO_000300: -3.23e-1

FS
type: SiteQuality
SIO_000300: 4.315e0

DP
type: SiteQuality
SIO_000300: 1.369216e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.042e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.17e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.71e-1

QD
type: SiteQuality
SIO_000300: 4.6e0

MQ
type: SiteQuality
SIO_000300: 5.489e1

GenotypeDepth
all individuals: 506
bin: 5.75e1
variant carriers: 5

GenotypeDepth
all individuals: 41
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 78
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7728
bin: 2.75e1
variant carriers: 50

GenotypeDepth
all individuals: 10070
bin: 1.75e1
variant carriers: 124

GenotypeDepth
all individuals: 217
bin: 6.75e1
variant carriers: 4

GenotypeDepth
all individuals: 152
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variant carriers: 1

GenotypeDepth
all individuals: 1241
bin: 4.75e1
variant carriers: 14

GenotypeDepth
all individuals: 1890
bin: 4.25e1
variant carriers: 23

GenotypeQuality
all individuals: 1061
bin: 3.25e1
variant carriers: 59

GenotypeQuality
all individuals: 211
bin: 9.25e1
variant carriers: 13

GenotypeQuality
all individuals: 464
bin: 6.75e1
variant carriers: 59

GenotypeQuality
all individuals: 1770
bin: 1.25e1
variant carriers: 79

GenotypeQuality
all individuals: 1584
bin: 2.25e1
variant carriers: 67

GenotypeQuality
all individuals: 3047
bin: 7.5e0
variant carriers: 85

GenotypeQuality
all individuals: 903
bin: 4.25e1
variant carriers: 66

GenotypeQuality
all individuals: 354
bin: 7.25e1
variant carriers: 32

GenotypeQuality
all individuals: 986
bin: 3.75e1
variant carriers: 61

GenotypeQuality
all individuals: 1131
bin: 2.75e1
variant carriers: 76

GenotypeQuality
all individuals: 1437
bin: 1.75e1
variant carriers: 94

GenotypeQuality
all individuals: 41772
bin: 2.5e0
variant carriers: 129

GenotypeQuality
all individuals: 304
bin: 7.75e1
variant carriers: 23

GenotypeQuality
all individuals: 247
bin: 8.25e1
variant carriers: 21

GenotypeQuality
all individuals: 556
bin: 5.75e1
variant carriers: 55

GenotypeQuality
all individuals: 493
bin: 6.25e1
variant carriers: 54

GenotypeQuality
all individuals: 666
bin: 5.25e1
variant carriers: 50

GenotypeQuality
all individuals: 219
bin: 8.75e1
variant carriers: 11

GenotypeQuality
all individuals: 785
bin: 4.75e1
variant carriers: 63

GenotypeQuality
all individuals: 1376
bin: 9.75e1
variant carriers: 109

South Asian
type: Population
allele count: 36
allele frequency: 2.236024844720497e-2
allele num: 1610
num of homozygotes: 4

European (Non-Finnish)
type: Population
allele count: 241
allele frequency: 2.085135836649939e-2
allele num: 11558
num of homozygotes: 1

Latino
type: Population
allele count: 28
allele frequency: 2.229299363057325e-2
allele num: 1256
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 15
allele frequency: 1.170046801872075e-2
allele num: 1282
num of homozygotes: 0

Other
type: Population
allele count: 8
allele frequency: 5.063291139240506e-2
allele num: 158
num of homozygotes: 0

East Asian
type: Population
allele count: 18
allele frequency: 2.261306532663317e-2
allele num: 796
num of homozygotes: 0

African
type: Population
allele count: 91
allele frequency: 6.190476190476191e-2
allele num: 1470
num of homozygotes: 10

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.042e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.17e0

MQ
type: SiteQuality
SIO_000300: 5.489e1

QD
type: SiteQuality
SIO_000300: 4.6e0

FS
type: SiteQuality
SIO_000300: 4.315e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.71e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.369216e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.23e-1

Other
type: Population
allele count: 2
allele frequency: 1.265822784810127e-2
allele num: 158
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 493
allele frequency: 4.265443848416681e-2
allele num: 11558
num of homozygotes: 0

East Asian
type: Population
allele count: 26
allele frequency: 3.266331658291458e-2
allele num: 796
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.315e0

QD
type: SiteQuality
SIO_000300: 4.6e0

VQSLOD
type: SiteQuality
SIO_000300: 5.17e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.042e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.71e-1

MQ
type: SiteQuality
SIO_000300: 5.489e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.23e-1

DP
type: SiteQuality
SIO_000300: 1.369216e6

GenotypeDepth
all individuals: 768
bin: 5.25e1
variant carriers: 31

GenotypeDepth
all individuals: 78
bin: 8.25e1
variant carriers: 9

GenotypeDepth
all individuals: 323
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 217
bin: 6.75e1
variant carriers: 27

GenotypeDepth
all individuals: 1241
bin: 4.75e1
variant carriers: 49

GenotypeDepth
all individuals: 9983
bin: 2.25e1
variant carriers: 312

GenotypeDepth
all individuals: 10070
bin: 1.75e1
variant carriers: 704

GenotypeDepth
all individuals: 97
bin: 7.75e1
variant carriers: 10

GenotypeDepth
all individuals: 41
bin: 9.25e1
variant carriers: 5

GenotypeQuality
all individuals: 211
bin: 9.25e1
variant carriers: 38

GenotypeQuality
all individuals: 1437
bin: 1.75e1
variant carriers: 211

GenotypeQuality
all individuals: 666
bin: 5.25e1
variant carriers: 297

GenotypeQuality
all individuals: 785
bin: 4.75e1
variant carriers: 376

GenotypeQuality
all individuals: 1061
bin: 3.25e1
variant carriers: 290

GenotypeQuality
all individuals: 219
bin: 8.75e1
variant carriers: 51

GenotypeQuality
all individuals: 304
bin: 7.75e1
variant carriers: 80

GenotypeQuality
all individuals: 1131
bin: 2.75e1
variant carriers: 271

GenotypeQuality
all individuals: 1770
bin: 1.25e1
variant carriers: 218