11-46389445-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389445
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389445
    reference: chr 11
allele count: 1
allele frequency: 1.083541012027305e-5
allele num: 92290
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.367-107C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1599C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3517C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+148C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.379-107C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.367-107C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.505C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.182-107C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.367-110C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.934-110C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000534215
  gene symbol: DGKZ
  hgvsc: ENST00000534215.1:n.563-107C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435332
  ensembl transcript: ENST00000525242
  gene symbol: DGKZ
  hgvsc: ENST00000525242.1:c.7-107C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1599C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.265-107C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.418-110C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.360-107C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.265-110C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.367-107C>G
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13530
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5028
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: African
reference allele: C
site quality: QD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum

11-46389445-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389445
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389445
    reference: chr 11
allele count: 1
allele frequency: 1.083541012027305e-5
allele num: 92290
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1599C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435332
  ensembl transcript: ENST00000525242
  gene symbol: DGKZ
  hgvsc: ENST00000525242.1:c.7-107C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.367-107C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.367-107C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3517C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.265-107C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+148C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000534215
  gene symbol: DGKZ
  hgvsc: ENST00000534215.1:n.563-107C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.360-107C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.934-110C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.379-107C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.505C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.367-110C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.418-110C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1599C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.265-110C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.182-107C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.367-107C>T
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21421
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD

11-46389447-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389447
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389447
    reference: chr 11
allele count: 1
allele frequency: 1.071765411986624e-5
allele num: 93304
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.360-105G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.507G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.418-108G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.934-108G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+150G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000534215
  gene symbol: DGKZ
  hgvsc: ENST00000534215.1:n.563-105G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3519G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.367-108G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1597G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.367-105G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1597G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.265-105G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.367-105G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.367-105G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435332
  ensembl transcript: ENST00000525242
  gene symbol: DGKZ
  hgvsc: ENST00000525242.1:c.7-105G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.182-105G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.379-105G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.265-108G>C
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6052
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

11-46389448-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389448
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389448
    reference: chr 11
allele count: 2
allele frequency: 2.121475698495874e-5
allele num: 94274
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.367-104G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+151G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.508G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.265-107G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000534215
  gene symbol: DGKZ
  hgvsc: ENST00000534215.1:n.563-104G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1596G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.360-104G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.182-104G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.367-104G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.934-107G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.367-107G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1596G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3520G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.265-104G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.379-104G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.418-107G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435332
  ensembl transcript: ENST00000525242
  gene symbol: DGKZ
  hgvsc: ENST00000525242.1:c.7-104G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.367-104G>A
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: African
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff

11-46389448-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389448
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389448
    reference: chr 11
allele count: 1301
allele frequency: 1.380019941871566e-2
allele num: 94274
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.367-104G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.418-107G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1596G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.367-104G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.367-107G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.360-104G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.508G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3520G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.379-104G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.367-104G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1596G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.265-104G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000534215
  gene symbol: DGKZ
  hgvsc: ENST00000534215.1:n.563-104G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.182-104G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.934-107G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+151G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435332
  ensembl transcript: ENST00000525242
  gene symbol: DGKZ
  hgvsc: ENST00000525242.1:c.7-104G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.265-107G>C
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 3.25e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 12058
  bin: 7.5e0
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 3.75e1
  variant carriers: 30
genotype quality: GenotypeQuality
num of homozygotes: 83
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ

11-46389450-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389450
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389450
    reference: chr 11
allele count: 1
allele frequency: 1.051369935025338e-5
allele num: 95114
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.418-105C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.934-105C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3522C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.367-105C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.367-102C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.182-102C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1594C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.379-102C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.367-102C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+153C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.510C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000534215
  gene symbol: DGKZ
  hgvsc: ENST00000534215.1:n.563-102C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.367-102C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.265-102C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1594C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.360-102C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.265-105C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435332
  ensembl transcript: ENST00000525242
  gene symbol: DGKZ
  hgvsc: ENST00000525242.1:c.7-102C>T
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11960
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6411
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23953
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum

11-46389458-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389458
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389458
    reference: chr 11
allele count: 1
allele frequency: 1.009387301907742e-5
allele num: 99070
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000534215
  gene symbol: DGKZ
  hgvsc: ENST00000534215.1:n.563-94T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.367-97T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435332
  ensembl transcript: ENST00000525242
  gene symbol: DGKZ
  hgvsc: ENST00000525242.1:c.7-94T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.367-94T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+161T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.360-94T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.182-94T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.418-97T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.518T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1586T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.379-94T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.367-94T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.265-97T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1586T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3530T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.367-94T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.934-97T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.265-94T>C
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10320
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

11-46389460-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389460
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389460
    reference: chr 11
allele count: 1
allele frequency: 9.989012086704625e-6
allele num: 100110
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.367-95C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.360-92C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.367-92C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000534215
  gene symbol: DGKZ
  hgvsc: ENST00000534215.1:n.563-92C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.520C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.367-92C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.418-95C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.265-92C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435332
  ensembl transcript: ENST00000525242
  gene symbol: DGKZ
  hgvsc: ENST00000525242.1:c.7-92C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.934-95C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.265-95C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.367-92C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1584C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3532C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+163C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1584C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.379-92C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.182-92C>T
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9804
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/11-46389477-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389477
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389477
    reference: chr 11
allele count: 1
allele frequency: 9.135924281459556e-6
allele num: 109458
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.418-78C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.367-78C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435332
  ensembl transcript: ENST00000525242
  gene symbol: DGKZ
  hgvsc: ENST00000525242.1:c.7-75C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.367-75C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+180C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1567C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.537C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.379-75C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.360-75C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.265-78C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.934-78C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.367-75C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.367-75C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3549C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000534215
  gene symbol: DGKZ
  hgvsc: ENST00000534215.1:n.563-75C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1567C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.182-75C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.265-75C>A
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4234
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

11-46389493-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389493
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389493
    reference: chr 11
allele count: 2
allele frequency: 1.707475326981525e-5
allele num: 117132
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.418-62G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.182-59G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1551G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000534215
  gene symbol: DGKZ
  hgvsc: ENST00000534215.1:n.563-59G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.367-62G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1551G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.367-59G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+196G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.379-59G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.553G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.934-62G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435332
  ensembl transcript: ENST00000525242
  gene symbol: DGKZ
  hgvsc: ENST00000525242.1:c.7-59G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.367-59G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.265-59G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.265-62G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.360-59G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.367-59G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3565G>A
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13215
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41522
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-46389494-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389494
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389494
    reference: chr 11
allele count: 1
allele frequency: 8.523550570225534e-6
allele num: 117322
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.265-58G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.367-58G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3566G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.360-58G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435332
  ensembl transcript: ENST00000525242
  gene symbol: DGKZ
  hgvsc: ENST00000525242.1:c.7-58G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.554G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1550G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.367-58G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000534215
  gene symbol: DGKZ
  hgvsc: ENST00000534215.1:n.563-58G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.367-61G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.367-58G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.934-61G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.182-58G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+197G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.265-61G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1550G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.418-61G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.379-58G>A
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41550
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13330
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1865
  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: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP

11-46389502-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389502
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389502
    reference: chr 11
allele count: 1
allele frequency: 8.391232839928842e-6
allele num: 119172
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000534215
  gene symbol: DGKZ
  hgvsc: ENST00000534215.1:n.563-50C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1542C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.418-53C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3574C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.367-50C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435332
  ensembl transcript: ENST00000525242
  gene symbol: DGKZ
  hgvsc: ENST00000525242.1:c.7-50C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.934-53C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1542C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.367-53C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+205C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.265-53C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.562C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.367-50C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.379-50C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.367-50C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.360-50C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.265-50C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.182-50C>G
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14245
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42483
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP

11-46389502-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389502
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389502
    reference: chr 11
allele count: 2
allele frequency: 1.678246567985768e-5
allele num: 119172
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3574C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000534215
  gene symbol: DGKZ
  hgvsc: ENST00000534215.1:n.563-50C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.367-53C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.934-53C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.182-50C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1542C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.379-50C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.367-50C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.367-50C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.562C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.418-53C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.367-50C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1542C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.265-53C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.360-50C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.265-50C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435332
  ensembl transcript: ENST00000525242
  gene symbol: DGKZ
  hgvsc: ENST00000525242.1:c.7-50C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+205C>T
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14245
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42483
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/11-46389514-AC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389514
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389513
    reference: chr 11
allele count: 6
allele frequency: 4.991763590076374e-5
allele num: 120198
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.934-39delC
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.418-39delC
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3588delC
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000534215
  gene symbol: DGKZ
  hgvsc: ENST00000534215.1:n.563-36delC
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.265-39delC
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.367-36delC
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.360-36delC
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.576delC
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.265-36delC
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.367-39delC
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435332
  ensembl transcript: ENST00000525242
  gene symbol: DGKZ
  hgvsc: ENST00000525242.1:c.7-36delC
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.367-36delC
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.182-36delC
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.367-36delC
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.379-36delC
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1528delC
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+219delC
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1528delC
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43020
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: AC
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

11-46389516-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389516
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389516
    reference: chr 11
allele count: 1
allele frequency: 8.314487162431821e-6
allele num: 120272
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435332
  ensembl transcript: ENST00000525242
  gene symbol: DGKZ
  hgvsc: ENST00000525242.1:c.7-36C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+219C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3588C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.367-36C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.379-36C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.182-36C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.576C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.265-39C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.367-36C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.367-39C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.418-39C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000534215
  gene symbol: DGKZ
  hgvsc: ENST00000534215.1:n.563-36C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1528C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.265-36C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1528C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.934-39C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.367-36C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.360-36C>G
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1949
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

11-46389518-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389518
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389518
    reference: chr 11
allele count: 1
allele frequency: 8.309512730173502e-6
allele num: 120344
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.367-37G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.367-34G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435332
  ensembl transcript: ENST00000525242
  gene symbol: DGKZ
  hgvsc: ENST00000525242.1:c.7-34G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+221G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.578G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.265-34G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.379-34G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.418-37G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3590G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.934-37G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000534215
  gene symbol: DGKZ
  hgvsc: ENST00000534215.1:n.563-34G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.360-34G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.367-34G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.265-37G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.367-34G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1526G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1526G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.182-34G>C
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43017
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum

11-46389525-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389525
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389525
    reference: chr 11
allele count: 1
allele frequency: 8.297928836962294e-6
allele num: 120512
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.182-27C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.367-27C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.265-27C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.367-27C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1519C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435332
  ensembl transcript: ENST00000525242
  gene symbol: DGKZ
  hgvsc: ENST00000525242.1:c.7-27C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+228C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000534215
  gene symbol: DGKZ
  hgvsc: ENST00000534215.1:n.563-27C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.360-27C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.418-30C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.585C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.367-30C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.265-30C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3597C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.934-30C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.367-27C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1519C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.379-27C>T
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/11-46389525-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389525
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389524
    reference: chr 11
allele count: 20
allele frequency: 1.659585767392459e-4
allele num: 120512
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435332
  ensembl transcript: ENST00000525242
  gene symbol: DGKZ
  hgvsc: ENST00000525242.1:c.7-26delA
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.367-26delA
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1518delA
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.586delA
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+229delA
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.367-26delA
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.265-29delA
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1518delA
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.182-26delA
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.367-29delA
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.418-29delA
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.367-26delA
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3598delA
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.265-26delA
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.379-26delA
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000534215
  gene symbol: DGKZ
  hgvsc: ENST00000534215.1:n.563-26delA
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.360-26delA
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.934-29delA
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: CA
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

11-46389535-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389535
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389535
    reference: chr 11
allele count: 1
allele frequency: 8.285690612312537e-6
allele num: 120690
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1509C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.360-17C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435332
  ensembl transcript: ENST00000525242
  gene symbol: DGKZ
  hgvsc: ENST00000525242.1:c.7-17C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.367-17C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.367-20C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.367-17C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.418-20C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.934-20C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1509C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+238C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.182-17C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.367-17C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000534215
  gene symbol: DGKZ
  hgvsc: ENST00000534215.1:n.563-17C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.595C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3607C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.265-20C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.265-17C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.379-17C>G
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff

11-46389542-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389542
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389542
    reference: chr 11
allele count: 2
allele frequency: 1.656095258599275e-5
allele num: 120766
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+245T>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000534215
  gene symbol: DGKZ
  hgvsc: ENST00000534215.1:n.563-10T>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.182-10T>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435332
  ensembl transcript: ENST00000525242
  gene symbol: DGKZ
  hgvsc: ENST00000525242.1:c.7-10T>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.265-10T>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3614T>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.934-13T>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.367-10T>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1502T>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1502T>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.367-10T>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.602T>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.367-13T>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.379-10T>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.265-13T>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.360-10T>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.418-13T>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.367-10T>G
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

11-46389563-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389563
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389563
    reference: chr 11
allele count: 1
allele frequency: 8.272530236098013e-6
allele num: 120882
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.273G>A
  hgvsp: ENST00000524984.1:c.273G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.623G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3635G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.390G>A
  hgvsp: ENST00000532868.2:c.390G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435332
  ensembl transcript: ENST00000525242
  gene symbol: DGKZ
  hgvsc: ENST00000525242.1:c.18G>A
  hgvsp: ENST00000525242.1:c.18G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1481G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.378G>A
  hgvsp: ENST00000318201.8:c.378G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.378G>A
  hgvsp: ENST00000421244.2:c.378G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.378G>A
  hgvsp: ENST00000527911.1:c.378G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.426G>A
  hgvsp: ENST00000343674.6:c.426G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.371G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.193G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.276G>A
  hgvsp: ENST00000395574.3:c.276G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.375G>A
  hgvsp: ENST00000456247.2:c.375G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1481G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+266G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.942G>A
  hgvsp: ENST00000454345.1:c.942G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val314Val
num of homozygotes: 0
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

11-46389565-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389565
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389565
    reference: chr 11
allele count: 1
allele frequency: 8.271982794275789e-6
allele num: 120890
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.625C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.377C>T
  hgvsp: ENSP00000395684.2:p.Ser126Phe
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1479C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+268C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1479C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.380C>T
  hgvsp: ENSP00000391021.2:p.Ser127Phe
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.278C>T
  hgvsp: ENSP00000378941.3:p.Ser93Phe
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.275C>T
  hgvsp: ENSP00000437060.1:p.Ser92Phe
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.392C>T
  hgvsp: ENSP00000436273.2:p.Ser131Phe
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.380C>T
  hgvsp: ENSP00000436291.1:p.Ser127Phe
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.195C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.380C>T
  hgvsp: ENSP00000320340.8:p.Ser127Phe
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3637C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.428C>T
  hgvsp: ENSP00000343065.6:p.Ser143Phe
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.944C>T
  hgvsp: ENSP00000412178.1:p.Ser315Phe
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435332
  ensembl transcript: ENST00000525242
  gene symbol: DGKZ
  hgvsc: ENST00000525242.1:c.20C>T
  hgvsp: ENSP00000435332.1:p.Ser7Phe
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.373C>T
  variant of: http://identifiers.org/hgnc/2857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15198
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43033
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser315Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

11-46389572-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389572
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389572
    reference: chr 11
allele count: 2
allele frequency: 1.654232353476369e-5
allele num: 120902
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3644A>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435332
  ensembl transcript: ENST00000525242
  gene symbol: DGKZ
  hgvsc: ENST00000525242.1:c.27A>G
  hgvsp: ENST00000525242.1:c.27A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.285A>G
  hgvsp: ENST00000395574.3:c.285A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.387A>G
  hgvsp: ENST00000421244.2:c.387A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1472A>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.387A>G
  hgvsp: ENST00000527911.1:c.387A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.399A>G
  hgvsp: ENST00000532868.2:c.399A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+275A>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.384A>G
  hgvsp: ENST00000456247.2:c.384A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.435A>G
  hgvsp: ENST00000343674.6:c.435A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1472A>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.387A>G
  hgvsp: ENST00000318201.8:c.387A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.380A>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.951A>G
  hgvsp: ENST00000454345.1:c.951A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.282A>G
  hgvsp: ENST00000524984.1:c.282A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.632A>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.202A>G
  variant of: http://identifiers.org/hgnc/2857
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15215
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg317Arg
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff

11-46389578-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389578
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389578
    reference: chr 11
allele count: 3
allele frequency: 2.48147167813658e-5
allele num: 120896
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.405C>T
  hgvsp: ENST00000532868.2:c.405C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.393C>T
  hgvsp: ENST00000527911.1:c.393C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.393C>T
  hgvsp: ENST00000421244.2:c.393C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.393C>T
  hgvsp: ENST00000318201.8:c.393C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.208C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.638C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+281C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.441C>T
  hgvsp: ENST00000343674.6:c.441C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435332
  ensembl transcript: ENST00000525242
  gene symbol: DGKZ
  hgvsc: ENST00000525242.1:c.33C>T
  hgvsp: ENST00000525242.1:c.33C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.288C>T
  hgvsp: ENST00000524984.1:c.288C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1466C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.390C>T
  hgvsp: ENST00000456247.2:c.390C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.386C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.957C>T
  hgvsp: ENST00000454345.1:c.957C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.291C>T
  hgvsp: ENST00000395574.3:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3650C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1466C>T
  variant of: http://identifiers.org/hgnc/2857
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42990
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys319Cys
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

11-46389583-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389583
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389583
    reference: chr 11
allele count: 1
allele frequency: 8.271161767381846e-6
allele num: 120902
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.398C>T
  hgvsp: ENSP00000436291.1:p.Ala133Val
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.446C>T
  hgvsp: ENSP00000343065.6:p.Ala149Val
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.391C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.213C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.398C>T
  hgvsp: ENSP00000320340.8:p.Ala133Val
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1461C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.296C>T
  hgvsp: ENSP00000378941.3:p.Ala99Val
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.410C>T
  hgvsp: ENSP00000436273.2:p.Ala137Val
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.643C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.962C>T
  hgvsp: ENSP00000412178.1:p.Ala321Val
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435332
  ensembl transcript: ENST00000525242
  gene symbol: DGKZ
  hgvsc: ENST00000525242.1:c.38C>T
  hgvsp: ENSP00000435332.1:p.Ala13Val
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.398C>T
  hgvsp: ENSP00000391021.2:p.Ala133Val
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3655C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+286C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.293C>T
  hgvsp: ENSP00000437060.1:p.Ala98Val
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1461C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.395C>T
  hgvsp: ENSP00000395684.2:p.Ala132Val
  variant of: http://identifiers.org/hgnc/2857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala321Val
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD

11-46389588-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389588
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389588
    reference: chr 11
allele count: 1
allele frequency: 8.271845945141119e-6
allele num: 120892
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+291A>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.967A>G
  hgvsp: ENSP00000412178.1:p.Lys323Glu
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.403A>G
  hgvsp: ENSP00000320340.8:p.Lys135Glu
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.415A>G
  hgvsp: ENSP00000436273.2:p.Lys139Glu
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.400A>G
  hgvsp: ENSP00000395684.2:p.Lys134Glu
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.451A>G
  hgvsp: ENSP00000343065.6:p.Lys151Glu
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1456A>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.403A>G
  hgvsp: ENSP00000436291.1:p.Lys135Glu
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.218A>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.396A>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.301A>G
  hgvsp: ENSP00000378941.3:p.Lys101Glu
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435332
  ensembl transcript: ENST00000525242
  gene symbol: DGKZ
  hgvsc: ENST00000525242.1:c.43A>G
  hgvsp: ENSP00000435332.1:p.Lys15Glu
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.403A>G
  hgvsp: ENSP00000391021.2:p.Lys135Glu
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.648A>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1456A>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.298A>G
  hgvsp: ENSP00000437060.1:p.Lys100Glu
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3660A>G
  variant of: http://identifiers.org/hgnc/2857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15244
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys323Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
reference allele: A
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

11-46389589-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389589
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389589
    reference: chr 11
allele count: 2
allele frequency: 1.654423929587718e-5
allele num: 120888
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435332
  ensembl transcript: ENST00000525242
  gene symbol: DGKZ
  hgvsc: ENST00000525242.1:c.44A>G
  hgvsp: ENSP00000435332.1:p.Lys15Arg
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.219A>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+292A>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1455A>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.302A>G
  hgvsp: ENSP00000378941.3:p.Lys101Arg
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.401A>G
  hgvsp: ENSP00000395684.2:p.Lys134Arg
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.416A>G
  hgvsp: ENSP00000436273.2:p.Lys139Arg
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.404A>G
  hgvsp: ENSP00000320340.8:p.Lys135Arg
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.404A>G
  hgvsp: ENSP00000391021.2:p.Lys135Arg
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1455A>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.299A>G
  hgvsp: ENSP00000437060.1:p.Lys100Arg
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.968A>G
  hgvsp: ENSP00000412178.1:p.Lys323Arg
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.404A>G
  hgvsp: ENSP00000436291.1:p.Lys135Arg
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.397A>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.649A>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3661A>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.452A>G
  hgvsp: ENSP00000343065.6:p.Lys151Arg
  variant of: http://identifiers.org/hgnc/2857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15243
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys323Arg
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-46389590-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389590
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389590
    reference: chr 11
allele count: 4
allele frequency: 3.309012094439205e-5
allele num: 120882
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.300G>T
  hgvsp: ENSP00000437060.1:p.Lys100Asn
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1454G>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1454G>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.405G>T
  hgvsp: ENSP00000436291.1:p.Lys135Asn
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.453G>T
  hgvsp: ENSP00000343065.6:p.Lys151Asn
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.405G>T
  hgvsp: ENSP00000391021.2:p.Lys135Asn
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.402G>T
  hgvsp: ENSP00000395684.2:p.Lys134Asn
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.303G>T
  hgvsp: ENSP00000378941.3:p.Lys101Asn
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.417G>T
  hgvsp: ENSP00000436273.2:p.Lys139Asn
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.650G>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.969G>T
  hgvsp: ENSP00000412178.1:p.Lys323Asn
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3662G>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.220G>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.398G>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.405G>T
  hgvsp: ENSP00000320340.8:p.Lys135Asn
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435332
  ensembl transcript: ENST00000525242
  gene symbol: DGKZ
  hgvsc: ENST00000525242.1:c.45G>T
  hgvsp: ENSP00000435332.1:p.Lys15Asn
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+293G>T
  variant of: http://identifiers.org/hgnc/2857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys323Asn
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

11-46389604-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389604
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389604
    reference: chr 11
allele count: 10
allele frequency: 8.279653579294243e-5
allele num: 120778
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.234C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.419C>G
  hgvsp: ENSP00000436291.1:p.Thr140Arg
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.317C>G
  hgvsp: ENSP00000378941.3:p.Thr106Arg
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.431C>G
  hgvsp: ENSP00000436273.2:p.Thr144Arg
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.416C>G
  hgvsp: ENSP00000395684.2:p.Thr139Arg
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.419C>G
  hgvsp: ENSP00000320340.8:p.Thr140Arg
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.314C>G
  hgvsp: ENSP00000437060.1:p.Thr105Arg
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.467C>G
  hgvsp: ENSP00000343065.6:p.Thr156Arg
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.983C>G
  hgvsp: ENSP00000412178.1:p.Thr328Arg
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1440C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.419C>G
  hgvsp: ENSP00000391021.2:p.Thr140Arg
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.664C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+307C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.412C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3676C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1440C>G
  variant of: http://identifiers.org/hgnc/2857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr328Arg
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

11-46389604-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389604
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389604
    reference: chr 11
allele count: 1
allele frequency: 8.279653579294243e-6
allele num: 120778
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.317C>T
  hgvsp: ENSP00000378941.3:p.Thr106Met
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1440C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1440C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.431C>T
  hgvsp: ENSP00000436273.2:p.Thr144Met
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.419C>T
  hgvsp: ENSP00000436291.1:p.Thr140Met
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.664C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3676C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.419C>T
  hgvsp: ENSP00000391021.2:p.Thr140Met
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.412C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.234C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.314C>T
  hgvsp: ENSP00000437060.1:p.Thr105Met
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.419C>T
  hgvsp: ENSP00000320340.8:p.Thr140Met
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+307C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.983C>T
  hgvsp: ENSP00000412178.1:p.Thr328Met
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.467C>T
  hgvsp: ENSP00000343065.6:p.Thr156Met
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.416C>T
  hgvsp: ENSP00000395684.2:p.Thr139Met
  variant of: http://identifiers.org/hgnc/2857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15244
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42801
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr328Met
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD

11-46389605-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389605
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389605
    reference: chr 11
allele count: 2
allele frequency: 1.65582103886212e-5
allele num: 120786
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1439G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.984G>A
  hgvsp: ENST00000454345.1:c.984G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.318G>A
  hgvsp: ENST00000395574.3:c.318G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.432G>A
  hgvsp: ENST00000532868.2:c.432G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+308G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.420G>A
  hgvsp: ENST00000527911.1:c.420G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.468G>A
  hgvsp: ENST00000343674.6:c.468G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.420G>A
  hgvsp: ENST00000421244.2:c.420G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.235G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1439G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.420G>A
  hgvsp: ENST00000318201.8:c.420G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.665G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.315G>A
  hgvsp: ENST00000524984.1:c.315G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.413G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3677G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.417G>A
  hgvsp: ENST00000456247.2:c.417G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr328Thr
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum

11-46389614-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389614
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389614
    reference: chr 11
allele count: 1
allele frequency: 8.286377195889957e-6
allele num: 120680
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.429C>T
  hgvsp: ENST00000421244.2:c.429C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+317C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.993C>T
  hgvsp: ENST00000454345.1:c.993C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.477C>T
  hgvsp: ENST00000343674.6:c.477C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.426C>T
  hgvsp: ENST00000456247.2:c.426C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1430C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.429C>T
  hgvsp: ENST00000318201.8:c.429C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.244C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.429C>T
  hgvsp: ENST00000527911.1:c.429C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.674C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.441C>T
  hgvsp: ENST00000532868.2:c.441C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3686C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.327C>T
  hgvsp: ENST00000395574.3:c.327C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.422C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1430C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.324C>T
  hgvsp: ENST00000524984.1:c.324C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2857
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42662
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile331Ile
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum

11-46389615-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389615
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389615
    reference: chr 11
allele count: 1
allele frequency: 8.290636555074699e-6
allele num: 120618
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+318G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.430G>A
  hgvsp: ENSP00000436291.1:p.Glu144Lys
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.427G>A
  hgvsp: ENSP00000395684.2:p.Glu143Lys
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.430G>A
  hgvsp: ENSP00000320340.8:p.Glu144Lys
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.325G>A
  hgvsp: ENSP00000437060.1:p.Glu109Lys
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.328G>A
  hgvsp: ENSP00000378941.3:p.Glu110Lys
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3687G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.245G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.478G>A
  hgvsp: ENSP00000343065.6:p.Glu160Lys
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.994G>A
  hgvsp: ENSP00000412178.1:p.Glu332Lys
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1429G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.430G>A
  hgvsp: ENSP00000391021.2:p.Glu144Lys
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.442G>A
  hgvsp: ENSP00000436273.2:p.Glu148Lys
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1429G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.675G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.423G>A
  variant of: http://identifiers.org/hgnc/2857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42594
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu332Lys
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

11-46389615-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389615
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389615
    reference: chr 11
allele count: 1
allele frequency: 8.290636555074699e-6
allele num: 120618
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.442G>C
  hgvsp: ENSP00000436273.2:p.Glu148Gln
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.675G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.994G>C
  hgvsp: ENSP00000412178.1:p.Glu332Gln
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+318G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.430G>C
  hgvsp: ENSP00000391021.2:p.Glu144Gln
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.325G>C
  hgvsp: ENSP00000437060.1:p.Glu109Gln
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.423G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.478G>C
  hgvsp: ENSP00000343065.6:p.Glu160Gln
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.427G>C
  hgvsp: ENSP00000395684.2:p.Glu143Gln
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.430G>C
  hgvsp: ENSP00000320340.8:p.Glu144Gln
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.328G>C
  hgvsp: ENSP00000378941.3:p.Glu110Gln
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.430G>C
  hgvsp: ENSP00000436291.1:p.Glu144Gln
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1429G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3687G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.245G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1429G>C
  variant of: http://identifiers.org/hgnc/2857
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42594
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu332Gln
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

11-46389641-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389641
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389641
    reference: chr 11
allele count: 1
allele frequency: 8.423322495325057e-6
allele num: 118718
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1403G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.1008+12G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.437+12G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3713G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.701G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.456+12G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.492+12G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.271G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.342+12G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.444+12G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1403G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+344G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.444+12G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.339+12G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.441+12G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.444+12G>C
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14887
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40431
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

11-46389646-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389646
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389646
    reference: chr 11
allele count: 2
allele frequency: 1.694943982101392e-5
allele num: 117998
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.706G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.456+17G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.444+17G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.276G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1398G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.444+17G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.342+17G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.492+17G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3718G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1398G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.444+17G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.339+17G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.441+17G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.1008+17G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+349G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.437+17G>A
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1737
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

11-46389648-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389648
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389648
    reference: chr 11
allele count: 1
allele frequency: 8.481620328747603e-6
allele num: 117902
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.1008+19T>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.492+19T>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.456+19T>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.339+19T>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.441+19T>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.437+19T>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.708T>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.278T>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3720T>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.444+19T>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+351T>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.444+19T>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.342+19T>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.444+19T>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1396T>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1396T>A
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39471
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

11-46389653-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389653
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389653
    reference: chr 11
allele count: 4
allele frequency: 3.437784691544768e-5
allele num: 116354
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.342+24C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+356C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.444+24C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.1008+24C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.492+24C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.283C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3725C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.713C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.444+24C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.456+24C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.437+24C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.441+24C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.444+24C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.339+24C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1391C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1391C>T
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37962
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2312
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

11-46389654-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389654
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389654
    reference: chr 11
allele count: 3
allele frequency: 2.579979360165119e-5
allele num: 116280
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.284C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.444+25C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.444+25C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.342+25C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.441+25C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.444+25C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1390C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.714C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+357C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.339+25C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.1008+25C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.492+25C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3726C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.437+25C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.456+25C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1390C>T
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2586
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum

11-46389655-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389655
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389655
    reference: chr 11
allele count: 1
allele frequency: 8.610149644400819e-6
allele num: 116142
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.342+26G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.441+26G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.715G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3727G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.339+26G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1389G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1389G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.444+26G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.492+26G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+358G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.285G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.444+26G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.456+26G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.437+26G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.444+26G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.1008+26G>A
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2359
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2011
  bin: 3.25e1
  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: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-46389656-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389656
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389656
    reference: chr 11
allele count: 8
allele frequency: 6.896908460782454e-5
allele num: 115994
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.444+27C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.716C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.456+27C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3728C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+359C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.342+27C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.437+27C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.492+27C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.441+27C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.286C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.444+27C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1388C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.444+27C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.339+27C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.1008+27C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1388C>T
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2791
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14707
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum

11-46389658-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389658
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389658
    reference: chr 11
allele count: 1
allele frequency: 8.692326414241508e-6
allele num: 115044
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.1008+29C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.288C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.718C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.444+29C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.444+29C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.444+29C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1386C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.441+29C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3730C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1386C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.437+29C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+361C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.342+29C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.339+29C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.492+29C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.456+29C>T
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2955
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36935
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

11-46389659-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389659
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389659
    reference: chr 11
allele count: 1
allele frequency: 8.728593125360055e-6
allele num: 114566
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+362C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.444+30C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.719C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3731C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.441+30C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.342+30C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.444+30C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1385C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.339+30C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.289C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1385C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.456+30C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.492+30C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.437+30C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.444+30C>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.1008+30C>G
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3500
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14326
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

11-46389661-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389661
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389661
    reference: chr 11
allele count: 2
allele frequency: 1.759045893507361e-5
allele num: 113698
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.291G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.437+32G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.444+32G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1383G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.456+32G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.444+32G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+364G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1383G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.441+32G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.342+32G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.1008+32G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.721G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.444+32G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.339+32G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3733G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.492+32G>A
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14048
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1762
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4011
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

11-46389663-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389663
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389663
    reference: chr 11
allele count: 1
allele frequency: 8.909320931558596e-6
allele num: 112242
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.723C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.444+34C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.444+34C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.441+34C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1381C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.342+34C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1381C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.492+34C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.293C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+366C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.456+34C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.437+34C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.444+34C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3735C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.1008+34C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.339+34C>T
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4871
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34433
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13696
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

11-46389664-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389664
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389665
    reference: chr 11
allele count: 4
allele frequency: 3.577689528102751e-5
allele num: 111804
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.492+38dupT
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1377dupT
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.441+38dupT
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.444+38dupT
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.1008+38dupT
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.297dupT
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.456+38dupT
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1377dupT
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.727dupT
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.444+38dupT
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.339+38dupT
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.444+38dupT
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.342+38dupT
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+370dupT
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.437+38dupT
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3739dupT
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

11-46389671-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389671
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389671
    reference: chr 11
allele count: 2
allele frequency: 1.853430700226118e-5
allele num: 107908
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.444+42T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.1008+42T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.492+42T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.441+42T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+374T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.731T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.437+42T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.301T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.444+42T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.444+42T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3743T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1373T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.339+42T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.456+42T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.342+42T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1373T>C
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7212
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6373
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

11-46389673-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389673
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389673
    reference: chr 11
allele count: 1
allele frequency: 9.400086480795623e-6
allele num: 106382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.303C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.733C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.444+44C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.456+44C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.492+44C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3745C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1371C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1371C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.339+44C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.444+44C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.437+44C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.1008+44C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.342+44C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.444+44C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.441+44C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+376C>T
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7957
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7047
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

11-46389678-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389678
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389678
    reference: chr 11
allele count: 7
allele frequency: 7.119754266767022e-5
allele num: 98318
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.444+49G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.441+49G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.437+49G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.1008+49G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.342+49G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.738G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3750G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.456+49G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.492+49G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.444+49G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.308G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1366G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.444+49G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.339+49G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+381G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1366G>A
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12167
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10781
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum

11-46389678-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389678
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389678
    reference: chr 11
allele count: 1
allele frequency: 1.017107752395289e-5
allele num: 98318
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.444+49G>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1366G>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.444+49G>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.437+49G>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+381G>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1366G>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.339+49G>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.1008+49G>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.308G>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.738G>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.342+49G>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3750G>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.444+49G>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.441+49G>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.456+49G>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.492+49G>T
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22848
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2762
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10781
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10137
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/11-46389681-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389681
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389681
    reference: chr 11
allele count: 1
allele frequency: 1.064962726304579e-5
allele num: 93900
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.311C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.456+52C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.1008+52C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3753C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1363C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.444+52C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.339+52C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.741C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+384C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1363C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.441+52C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.492+52C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.444+52C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.437+52C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.342+52C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.444+52C>A
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2968
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9062
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12620
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

11-46389689-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389689
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389689
    reference: chr 11
allele count: 94
allele frequency: 1.10650720406818e-3
allele num: 84952
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1355G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.444+60G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.437+60G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+392G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.492+60G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3761G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.444+60G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.444+60G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.441+60G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1355G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.319G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.749G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.456+60G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.342+60G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.1008+60G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.339+60G>A
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 16741
  bin: 1.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2956
  bin: 1.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 6779
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 16245
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15518
  bin: 2.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

11-46389690-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389690
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389690
    reference: chr 11
allele count: 9
allele frequency: 1.083449703857081e-4
allele num: 83068
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.444+61C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.444+61C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.456+61C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.444+61C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1354C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.492+61C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.342+61C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.750C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+393C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.320C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3762C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1354C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.441+61C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.1008+61C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.437+61C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.339+61C>T
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16943
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17085
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2880
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

11-46389691-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389691
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389691
    reference: chr 11
allele count: 103
allele frequency: 1.252949906332871e-3
allele num: 82206
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3763G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.492+62G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.444+62G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1353G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.1008+62G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1353G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+394G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.751G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.321G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.441+62G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.444+62G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.339+62G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.444+62G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.342+62G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.456+62G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.437+62G>A
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2739
  bin: 1.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 14597
  bin: 2.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6385
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 1
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

11-46389697-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389697
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389697
    reference: chr 11
allele count: 3
allele frequency: 3.91644908616188e-5
allele num: 76600
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.1008+68A>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.342+68A>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1347A>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.757A>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.444+68A>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+400A>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.327A>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1347A>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.444+68A>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.456+68A>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3769A>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.444+68A>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.437+68A>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.441+68A>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.339+68A>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.492+68A>T
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17842
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12477
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2718
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

11-46389701-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389701
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389701
    reference: chr 11
allele count: 1
allele frequency: 1.385502105963201e-5
allele num: 72176
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.761C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.339+72C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.456+72C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.492+72C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.441+72C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3773C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.342+72C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.444+72C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.331C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1343C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+404C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1343C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.437+72C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.444+72C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.444+72C>T
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.1008+72C>T
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3733
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4945
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10873
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20235
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2126
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

11-46389707-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389707
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389707
    reference: chr 11
allele count: 1
allele frequency: 1.530596626565035e-5
allele num: 65334
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.441+78G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.456+78G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1337G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.444+78G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.767G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.444+78G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.444+78G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.342+78G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.492+78G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.437+78G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3779G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.337G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.339+78G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.1008+78G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+410G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1337G>A
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8967
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21397
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

11-46389711-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389711
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389711
    reference: chr 11
allele count: 1
allele frequency: 1.686226898691488e-5
allele num: 59304
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1333T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.444+82T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.342+82T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.441+82T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+414T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.771T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.339+82T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3783T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.456+82T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.444+82T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.341T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.444+82T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.1008+82T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.492+82T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1333T>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.437+82T>C
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21807
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7966
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16220
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP

11-46389728-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389728
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389728
    reference: chr 11
allele count: 1
allele frequency: 2.512057877813505e-5
allele num: 39808
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3800G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.788G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.441+99G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.444+99G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.1008+99G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1316G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.358G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.437+99G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.444+99G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.339+99G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.444+99G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.456+99G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.492+99G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1316G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+431G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.342+99G>C
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6423
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9711
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum

11-46389729-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389729
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389729
    reference: chr 11
allele count: 7
allele frequency: 1.757910597689603e-4
allele num: 39820
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.444+100A>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.342+100A>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.444+100A>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.359A>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.441+100A>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+432A>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.456+100A>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.492+100A>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.437+100A>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1315A>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.789A>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3801A>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.1008+100A>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.339+100A>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1315A>G
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.444+100A>G
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9645
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18406
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20783
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/11-46389735-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389735
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389735
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 33906
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.1008+106C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.456+106C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.365C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.492+106C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.342+106C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.444+106C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1309C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3807C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1309C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.795C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.441+106C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.339+106C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.444+106C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.444+106C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+438C>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.437+106C>A
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7737
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17762
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23264
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5899
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

11-46389738-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389738
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389738
    reference: chr 11
allele count: 1
allele frequency: 3.271180896303566e-5
allele num: 30570
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.444+109G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.437+109G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1306G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3810G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1306G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.368G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.456+109G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.492+109G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.798G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+441G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.444+109G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.342+109G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.441+109G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.1008+109G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.444+109G>A
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.339+109G>A
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5768
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6308
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum

11-46389738-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46389738
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 46389738
    reference: chr 11
allele count: 1
allele frequency: 3.271180896303566e-5
allele num: 30570
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436273
  ensembl transcript: ENST00000532868
  gene symbol: DGKZ
  hgvsc: ENST00000532868.2:c.456+109G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000437060
  ensembl transcript: ENST00000524984
  gene symbol: DGKZ
  hgvsc: ENST00000524984.1:c.339+109G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000438417
  ensembl transcript: ENST00000543978
  gene symbol: DGKZ
  hgvsc: ENST00000543978.1:c.166+3810G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435435
  ensembl transcript: ENST00000533376
  gene symbol: DGKZ
  hgvsc: ENST00000533376.1:c.162-1306G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000527674
  gene symbol: DGKZ
  hgvsc: ENST00000527674.1:n.798G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000435763
  ensembl transcript: ENST00000524448
  gene symbol: DGKZ
  hgvsc: ENST00000524448.1:c.96+441G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000391021
  ensembl transcript: ENST00000421244
  gene symbol: DGKZ
  hgvsc: ENST00000421244.2:c.444+109G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000436291
  ensembl transcript: ENST00000527911
  gene symbol: DGKZ
  hgvsc: ENST00000527911.1:c.444+109G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000528173
  gene symbol: DGKZ
  hgvsc: ENST00000528173.1:n.368G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000378941
  ensembl transcript: ENST00000395574
  gene symbol: DGKZ
  hgvsc: ENST00000395574.3:c.342+109G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000320340
  ensembl transcript: ENST00000318201
  gene symbol: DGKZ
  hgvsc: ENST00000318201.8:c.444+109G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000343065
  ensembl transcript: ENST00000343674
  gene symbol: DGKZ
  hgvsc: ENST00000343674.6:c.492+109G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000434719
  ensembl transcript: ENST00000528615
  gene symbol: DGKZ
  hgvsc: ENST00000528615.1:c.-222-1306G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000395684
  ensembl transcript: ENST00000456247
  gene symbol: DGKZ
  hgvsc: ENST00000456247.2:c.441+109G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl protein: ENSP00000412178
  ensembl transcript: ENST00000454345
  gene symbol: DGKZ
  hgvsc: ENST00000454345.1:c.1008+109G>C
  variant of: http://identifiers.org/hgnc/2857
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149091
  ensembl transcript: ENST00000531879
  gene symbol: DGKZ
  hgvsc: ENST00000531879.1:n.437+109G>C
  variant of: http://identifiers.org/hgnc/2857
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2616
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16477
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5768
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
reference allele: G

GenotypeDepth
all individuals: 9
bin: 5.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1310
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5793
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12784
bin: 7.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 694
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 7.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 21421
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 4222
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1350
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 470
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 848
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4478
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23934
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1081
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17613
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2565
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 533
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1541
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 952
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7796
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50694
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6272
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14722
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 704
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4972
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.402524544179523e-4
allele num: 7130
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.668e1

DP
type: SiteQuality
SIO_000300: 9.94161e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 9.09e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.02e0

VQSLOD
type: SiteQuality
SIO_000300: 1.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.856e0

GenotypeDepth
all individuals: 2
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5028
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12784
bin: 7.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 13530
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 7.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 694
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 5793
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4478
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4222
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1081
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1350
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 470
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 533
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2565
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17613
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23934
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 952
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1541
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 246
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 848
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50694
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 704
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.792555359326178e-5
allele num: 14722
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4972
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 7796
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6272
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7130
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.09e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

BaseQRankSum
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SIO_000300: -1.856e0

DP
type: SiteQuality
SIO_000300: 9.94161e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.02e0

VQSLOD
type: SiteQuality
SIO_000300: 1.65e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.668e1

GenotypeDepth
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bin: 2.5e0
variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

South Asian
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allele frequency: 6.764984440535787e-5
allele num: 14782
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6348
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7254
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7942
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 51220
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5042
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 716
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.829e1

MQRankSum
type: SiteQuality
SIO_000300: -4.79e-1

InbreedingCoeff
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SIO_000300: -3.7e-3

ClippingRankSum
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SIO_000300: 3.7e-2

FS
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SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: -1.11e-1

DP
type: SiteQuality
SIO_000300: 1.011507e6

VQSLOD
type: SiteQuality
SIO_000300: -1.736e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.05e-1

QD
type: SiteQuality
SIO_000300: 2.157e1

GenotypeDepth
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bin: 1.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 23
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.941069140882798e-5
allele num: 51518
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8024
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6388
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5056
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 730
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.748549061951681e-5
allele num: 14818
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7740
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.883e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.89e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.72e-1

DP
type: SiteQuality
SIO_000300: 1.026394e6

QD
type: SiteQuality
SIO_000300: 1.66e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.439999999999999e-2

GenotypeDepth
all individuals: 11
bin: 6.75e1
variant carriers: 10

GenotypeDepth
all individuals: 26
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variant carriers: 23

GenotypeDepth
all individuals: 6156
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variant carriers: 132

GenotypeDepth
all individuals: 4902
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variant carriers: 353

GenotypeDepth
all individuals: 4
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variant carriers: 4

GenotypeDepth
all individuals: 4
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variant carriers: 4

GenotypeDepth
all individuals: 22960
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variant carriers: 249

GenotypeDepth
all individuals: 3
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variant carriers: 2

GenotypeDepth
all individuals: 40
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variant carriers: 32

GenotypeDepth
all individuals: 12474
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GenotypeDepth
all individuals: 7
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variant carriers: 7

GenotypeDepth
all individuals: 21
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variant carriers: 20

GenotypeDepth
all individuals: 26
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variant carriers: 24

GenotypeDepth
all individuals: 5
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variant carriers: 5

GenotypeDepth
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variant carriers: 1

GenotypeQuality
all individuals: 2375
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variant carriers: 10

GenotypeQuality
all individuals: 284
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variant carriers: 2

GenotypeQuality
all individuals: 176
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variant carriers: 14

GenotypeQuality
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variant carriers: 5

GenotypeQuality
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variant carriers: 15

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1133

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 11

GenotypeQuality
all individuals: 411
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GenotypeQuality
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variant carriers: 10

GenotypeQuality
all individuals: 23
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variant carriers: 17

GenotypeQuality
all individuals: 880
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variant carriers: 12

Latino
type: Population
allele count: 66
allele frequency: 8.225324027916252e-3
allele num: 8024
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5056
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 16
allele frequency: 3.105710625412477e-4
allele num: 51518
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6388
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.748549061951681e-5
allele num: 14818
num of homozygotes: 0

African
type: Population
allele count: 1215
allele frequency: 1.569767441860465e-1
allele num: 7740
num of homozygotes: 83

Other
type: Population
allele count: 3
allele frequency: 4.10958904109589e-3
allele num: 730
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.439999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.89e0

QD
type: SiteQuality
SIO_000300: 1.66e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.7e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.45e-1

DP
type: SiteQuality
SIO_000300: 1.026394e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.72e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.883e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 14
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variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7854
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8142
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 742
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.963093835885355e-4
allele num: 5094
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6464
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51966
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.033866e6

MQRankSum
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SIO_000300: 7.41e-1

MQ
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SIO_000300: 5.641e1

ClippingRankSum
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BaseQRankSum
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QD
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InbreedingCoeff
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SIO_000300: -3.9e-3

VQSLOD
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FS
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SIO_000300: 2.596e0

ReadPosRankSum
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SIO_000300: -7.41e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 286
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5340
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.844950370835025e-5
allele num: 54202
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15042
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8238
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8738
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 766
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -9.062e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.71e-1

BaseQRankSum
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SIO_000300: 3.42e0

DP
type: SiteQuality
SIO_000300: 1.099617e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
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SIO_000300: -2.89e-1

MQ
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SIO_000300: 6.0e1

ClippingRankSum
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SIO_000300: 3.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.3e-3

QD
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SIO_000300: 6.48e0

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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South Asian
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allele frequency: 6.610259122157589e-5
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Latino
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European (Non-Finnish)
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allele frequency: 0.0e0
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African
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East Asian
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Other
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European (Finnish)
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allele frequency: 0.0e0
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MQRankSum
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BaseQRankSum
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MQ
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FS
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InbreedingCoeff
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DP
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VQSLOD
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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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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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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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African
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Other
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Latino
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 59946
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FS
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MQ
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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DP
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MQRankSum
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VQSLOD
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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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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

African
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East Asian
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Other
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Latino
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European (Non-Finnish)
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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DP
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SIO_000300: 1.361429e6

MQRankSum
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FS
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MQ
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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QD
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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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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele num: 8454
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African
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European (Non-Finnish)
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allele frequency: 0.0e0
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European (Finnish)
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Latino
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num of homozygotes: 0

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

Latino
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African
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European (Finnish)
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European (Non-Finnish)
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East Asian
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DP
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MQRankSum
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InbreedingCoeff
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MQ
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VQSLOD
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QD
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FS
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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European (Finnish)
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Other
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South Asian
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VQSLOD
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ClippingRankSum
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DP
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QD
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MQ
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BaseQRankSum
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FS
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MQRankSum
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ReadPosRankSum
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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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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 (Non-Finnish)
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allele num: 65940
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European (Finnish)
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South Asian
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East Asian
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African
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Latino
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Other
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FS
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InbreedingCoeff
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DP
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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MQ
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VQSLOD
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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European (Finnish)
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South Asian
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Latino
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East Asian
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VQSLOD
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ClippingRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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QD
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MQRankSum
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MQ
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DP
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BaseQRankSum
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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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African
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Other
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East Asian
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European (Non-Finnish)
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South Asian
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European (Finnish)
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Latino
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FS
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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MQRankSum
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MQ
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BaseQRankSum
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InbreedingCoeff
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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Latino
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European (Non-Finnish)
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European (Finnish)
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East Asian
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FS
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ClippingRankSum
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QD
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InbreedingCoeff
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MQRankSum
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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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GenotypeDepth
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GenotypeDepth
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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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bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.510847887834653e-5
allele num: 66188
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
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allele count: 0
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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European (Finnish)
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allele count: 2
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Other
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East Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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South Asian
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MQ
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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FS
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InbreedingCoeff
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MQRankSum
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DP
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ClippingRankSum
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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num of homozygotes: 0

African
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
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allele num: 66328
num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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: 1
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allele num: 66332
num of homozygotes: 0

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

South Asian
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East Asian
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allele frequency: 0.0e0
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African
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Other
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.014772384684956e-5
allele num: 66340
num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 1.543829314231019e-5
allele num: 64774
num of homozygotes: 0

African
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allele frequency: 0.0e0
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Latino
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allele frequency: 8.837044892188053e-5
allele num: 11316
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European (Finnish)
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allele frequency: 0.0e0
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Other
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East Asian
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MQRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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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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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele num: 8520
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South Asian
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FS
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QD
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VQSLOD
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ClippingRankSum
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MQRankSum
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DP
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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MQ
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SIO_000300: 5.954e1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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European (Non-Finnish)
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allele num: 63926
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East Asian
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African
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Other
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Latino
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South Asian
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MQ
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SIO_000300: 5.945e1

VQSLOD
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QD
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FS
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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European (Finnish)
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South Asian
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African
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European (Non-Finnish)
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ClippingRankSum
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VQSLOD
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QD
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ReadPosRankSum
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FS
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MQ
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InbreedingCoeff
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DP
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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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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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South Asian
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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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InbreedingCoeff
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FS
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MQ
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DP
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MQRankSum
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BaseQRankSum
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QD
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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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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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African
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Latino
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East Asian
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European (Finnish)
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South Asian
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MQRankSum
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DP
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FS
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ReadPosRankSum
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SIO_000300: -4.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.72e0

MQ
type: SiteQuality
SIO_000300: 5.941e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.2e-2

QD
type: SiteQuality
SIO_000300: 1.243e1

InbreedingCoeff
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SIO_000300: -8.0e-4

BaseQRankSum
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SIO_000300: -1.806e0

GenotypeDepth
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variant carriers: 0

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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bin: 3.25e1
variant carriers: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.58122766515923e-5
allele num: 63242
num of homozygotes: 0

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

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

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

ReadPosRankSum
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SIO_000300: 1.06e0

VQSLOD
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FS
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QD
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InbreedingCoeff
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ClippingRankSum
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MQ
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SIO_000300: 5.928e1

BaseQRankSum
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SIO_000300: -7.64e-1

MQRankSum
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DP
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GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63002
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6052
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele frequency: 6.29643621710112e-5
allele num: 15882
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VQSLOD
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SIO_000300: -1.397e0

MQRankSum
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SIO_000300: 1.05e0

ReadPosRankSum
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SIO_000300: 5.73e-1

QD
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BaseQRankSum
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SIO_000300: -2.054e0

FS
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SIO_000300: 4.618e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.5e-2

InbreedingCoeff
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SIO_000300: -9.0e-4

MQ
type: SiteQuality
SIO_000300: 5.79e1

DP
type: SiteQuality
SIO_000300: 1.32989e6

GenotypeDepth
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variant carriers: 0

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

Latino
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allele frequency: 0.0e0
allele num: 10856
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.198976327575176e-5
allele num: 62520
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 2.698e0

MQRankSum
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SIO_000300: 1.72e0

BaseQRankSum
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SIO_000300: -1.592e0

InbreedingCoeff
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ClippingRankSum
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DP
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QD
type: SiteQuality
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VQSLOD
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ReadPosRankSum
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MQ
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Non-Finnish)
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allele count: 1
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allele num: 61756
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European (Finnish)
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allele frequency: 0.0e0
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African
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East Asian
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Latino
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allele frequency: 0.0e0
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South Asian
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VQSLOD
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InbreedingCoeff
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FS
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QD
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ReadPosRankSum
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MQRankSum
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MQ
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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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GenotypeQuality
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European (Non-Finnish)
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European (Finnish)
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Latino
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African
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South Asian
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East Asian
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Other
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MQRankSum
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DP
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QD
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MQ
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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FS
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VQSLOD
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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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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 count: 2
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allele num: 59568
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Other
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Latino
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allele count: 0
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European (Finnish)
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East Asian
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African
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South Asian
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InbreedingCoeff
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MQRankSum
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FS
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DP
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SIO_000300: 1.229591e6

VQSLOD
type: SiteQuality
SIO_000300: 6.8e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.646e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.27e0

QD
type: SiteQuality
SIO_000300: 1.117e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.99e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 786
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.371365880416895e-4
allele num: 7292
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8910
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5450
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9988
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58782
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.553e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.772e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.97e0

VQSLOD
type: SiteQuality
SIO_000300: -9.227e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e-2

DP
type: SiteQuality
SIO_000300: 1.210258e6

GenotypeDepth
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variant carriers: 4

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 7

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8814
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14514
num of homozygotes: 0

East Asian
type: Population
allele count: 7
allele frequency: 1.072632546736132e-3
allele num: 6526
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 730
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8286
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4876
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54572
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.4e-2

VQSLOD
type: SiteQuality
SIO_000300: 7.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.19e-1

DP
type: SiteQuality
SIO_000300: 1.091748e6

QD
type: SiteQuality
SIO_000300: 1.065e1

MQRankSum
type: SiteQuality
SIO_000300: -2.27e-1

FS
type: SiteQuality
SIO_000300: 2.841e0

MQ
type: SiteQuality
SIO_000300: 5.945e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.852e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4876
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14514
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.206854936036688e-4
allele num: 8286
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8814
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54572
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 730
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6526
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.27e-1

DP
type: SiteQuality
SIO_000300: 1.091748e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.852e0

VQSLOD
type: SiteQuality
SIO_000300: 7.44e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.4e-2

FS
type: SiteQuality
SIO_000300: 2.841e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.19e-1

MQ
type: SiteQuality
SIO_000300: 5.945e1

QD
type: SiteQuality
SIO_000300: 1.065e1

GenotypeDepth
all individuals: 3
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 43
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7956
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.088176920895946e-5
allele num: 14108
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6172
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8240
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4618
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 710
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52096
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.918e1

QD
type: SiteQuality
SIO_000300: 1.138e1

MQRankSum
type: SiteQuality
SIO_000300: 1.91e0

VQSLOD
type: SiteQuality
SIO_000300: -4.477e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.36e-1

FS
type: SiteQuality
SIO_000300: 1.779e0

BaseQRankSum
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SIO_000300: -3.039e0

DP
type: SiteQuality
SIO_000300: 1.036404e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.97e-1

GenotypeDepth
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variant carriers: 4

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4046
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.836884643644379e-4
allele num: 5444
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Other
type: Population
allele count: 1
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allele num: 646
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Latino
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allele count: 14
allele frequency: 1.940670917660105e-3
allele num: 7214
num of homozygotes: 0

African
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allele count: 9
allele frequency: 1.246537396121884e-3
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South Asian
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allele count: 30
allele frequency: 2.236469360369763e-3
allele num: 13414
num of homozygotes: 0

European (Non-Finnish)
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allele count: 39
allele frequency: 8.30352580480327e-4
allele num: 46968
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.65e-1

BaseQRankSum
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MQRankSum
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SIO_000300: 2.63e-1

MQ
type: SiteQuality
SIO_000300: 5.93e1

QD
type: SiteQuality
SIO_000300: 1.259e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

FS
type: SiteQuality
SIO_000300: 6.04e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.76e0

DP
type: SiteQuality
SIO_000300: 9.28951e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.1e-1

GenotypeDepth
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variant carriers: 1

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3958
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.541077969649399e-5
allele num: 45864
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 5.706134094151213e-4
allele num: 7010
num of homozygotes: 0

East Asian
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allele count: 0
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South Asian
type: Population
allele count: 2
allele frequency: 1.507840772014475e-4
allele num: 13264
num of homozygotes: 0

African
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Other
type: Population
allele count: 0
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MQ
type: SiteQuality
SIO_000300: 5.906e1

InbreedingCoeff
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SIO_000300: -6.5e-3

QD
type: SiteQuality
SIO_000300: 1.217e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.37e0

FS
type: SiteQuality
SIO_000300: 6.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.13e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.79e-1

DP
type: SiteQuality
SIO_000300: 9.05255e5

GenotypeDepth
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variant carriers: 3

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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variant carriers: 18

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 98

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5206
num of homozygotes: 0

South Asian
type: Population
allele count: 93
allele frequency: 7.055075102412381e-3
allele num: 13182
num of homozygotes: 1

Latino
type: Population
allele count: 1
allele frequency: 1.446759259259259e-4
allele num: 6912
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3906
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6992
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.982640877649028e-4
allele num: 45394
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.94e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.868e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.2e-3

DP
type: SiteQuality
SIO_000300: 9.0628e5

ClippingRankSum
type: SiteQuality
SIO_000300: -2.31e-1

FS
type: SiteQuality
SIO_000300: 1.913e0

MQRankSum
type: SiteQuality
SIO_000300: 3.52e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.38e0

QD
type: SiteQuality
SIO_000300: 1.223e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 554
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4776
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6274
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.567398119122257e-4
allele num: 12760
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.379819133745835e-5
allele num: 42020
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.699999999999999e-3

MQRankSum
type: SiteQuality
SIO_000300: 5.47e-1

DP
type: SiteQuality
SIO_000300: 8.41174e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.45e0

FS
type: SiteQuality
SIO_000300: 6.536e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.43e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.15e-1

QD
type: SiteQuality
SIO_000300: 9.99e0

MQ
type: SiteQuality
SIO_000300: 5.911e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.2e-2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5804
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3380
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4326
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12408
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.533698185872099e-5
allele num: 39468
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6248
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 542
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.65e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.65e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 8.02841e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.13e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

QD
type: SiteQuality
SIO_000300: 1.218e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.04e0

GenotypeDepth
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variant carriers: 1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5750
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5050
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35438
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 3.405994550408719e-4
allele num: 2936
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 506
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3788
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.4433e5

VQSLOD
type: SiteQuality
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QD
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.54e-2

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3294
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.12832384408434e-5
allele num: 31966
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4336
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 472
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South Asian
type: Population
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: 2612
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: 1.49e0

VQSLOD
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FS
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ReadPosRankSum
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ClippingRankSum
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SIO_000300: -9.19e-1

InbreedingCoeff
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QD
type: SiteQuality
SIO_000300: 1.985e1

MQRankSum
type: SiteQuality
SIO_000300: -7.78e-1

DP
type: SiteQuality
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GenotypeDepth
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 346
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.843553230650005e-5
allele num: 20646
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3826
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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

QD
type: SiteQuality
SIO_000300: 2.989e1

VQSLOD
type: SiteQuality
SIO_000300: -3.108e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.36e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.32e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.84e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.56e0

DP
type: SiteQuality
SIO_000300: 5.62472e5

MQ
type: SiteQuality
SIO_000300: 5.972e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.96e0

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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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 3820
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 3.387533875338753e-4
allele num: 20664
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 1774
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9754
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 2036
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 346
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1426
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.843e1

MQRankSum
type: SiteQuality
SIO_000300: -2.51e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.715e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: -1.09e-1

InbreedingCoeff
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SIO_000300: -3.82e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.48e-1

QD
type: SiteQuality
SIO_000300: 1.258e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.73e-1

DP
type: SiteQuality
SIO_000300: 5.61575e5

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 314
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 3294
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9260
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1072
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1428
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 17170
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -3.168e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.85e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.741e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.48e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.48e-1

QD
type: SiteQuality
SIO_000300: 2.048e1

DP
type: SiteQuality
SIO_000300: 5.088e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.393e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15122
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 286
num of homozygotes: 0

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

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 1.113833815994654e-4
allele num: 8978
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.36e-1

DP
type: SiteQuality
SIO_000300: 4.80653e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.0e0

QD
type: SiteQuality
SIO_000300: 1.175e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.04e-2

VQSLOD
type: SiteQuality
SIO_000300: -7.161999999999999e-1

FS
type: SiteQuality
SIO_000300: 2.971e0

MQRankSum
type: SiteQuality
SIO_000300: 1.35e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.85e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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